WO2012171335A1 - Multi-vinylsulfone containing molecule - Google Patents
Multi-vinylsulfone containing molecule Download PDFInfo
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- WO2012171335A1 WO2012171335A1 PCT/CN2012/000827 CN2012000827W WO2012171335A1 WO 2012171335 A1 WO2012171335 A1 WO 2012171335A1 CN 2012000827 W CN2012000827 W CN 2012000827W WO 2012171335 A1 WO2012171335 A1 WO 2012171335A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/74—Synthetic polymeric materials
- A61K31/795—Polymers containing sulfur
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
- A61K31/573—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/095—Sulfur, selenium, or tellurium compounds, e.g. thiols
- A61K31/10—Sulfides; Sulfoxides; Sulfones
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/716—Glucans
- A61K31/721—Dextrans
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/726—Glycosaminoglycans, i.e. mucopolysaccharides
- A61K31/728—Hyaluronic acid
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
- A61K31/734—Alginic acid
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/22—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against growth factors ; against growth regulators
Definitions
- This disclosure generally relates to generation of a multi-vinylsulfone molecule and to applications of the multi-vinylsulfone containing molecule.
- hydroxyl-bearing water soluble polymers include: hyaluranic acid (HA), polyethylene glycol (PEG), dextran, polyvinyl alcohol, alginate, cyclodextrin, and the like. Hydroxyl-bearing water soluble polymers are generally non-toxic, and the hydroxyl groups generally allow these polymers to be soluble in an aqueous environment. However, hydroxyl- bearing water soluble polymers alone do not usually have functionality toward animal cells or tissues and must be modified with an active agent to exhibit functionality toward animal cells or tissues.
- hydroxyl-bearing water soluble polymers can be linked with hydrophobic anti-cancer drugs to increase the solubility and targeting of the anticancer drug.
- Hydroxyl-bearing water soluble polymers can be linked with proteins or other labile
- the hydroxyl-bearing water soluble polymer can also be modified for use as a hydrogel.
- a hydrogel made with a modified hydroxyl-bearing water soluble polymer can be used, for example, in a tissue engineering scaffold, a drug delivery depot, a drug carrier in polymer-drug conjugates, as well as other biomedical applications. Modifying hydroxyl-bearing water soluble polymers for use in a hydrogel traditionally involves complicated chemistry and harsh conditions, which may be expensive and not suitable for biomedical applications.
- hydroxyl-bearing water soluble polymer modified with two or more vinylsulfone groups can be combined with an active agent and/or form crosslinks between polymers at in aqueous medium at mild physiological conditions of a pH of about 7.4, a pressure of about 1 atm, or a temperature of about 37 degrees Celsius.
- a method of forming the modified polymer is described, according to an embodiment.
- a water soluble polymer containing a hydroxyl group is dissolved in an aqueous solution to form a polymer solution.
- a molecule containing two vinylsulfone groups is added to the polymer solution.
- the modified polymer is formed by controlling a number of the vinylsulfone groups that are grafted to the polymer.
- the vinylsulfone groups are chemically reactive.
- a hydrogel that can be made from the modified polymer.
- the hydrogel includes the modified polymer (a multi- vinylsulfone containing molecule) and a multi-thiol containing molecule.
- the hydrogel is formed at a site of a biological tissue upon delivery to the site.
- the hydrogel is formed from an aqueous solution that includes the modified polymer and the multi-thiol containing molecule by a covalent bond between the modified polymer and the multi-thiol containing molecule.
- a drug delivery system includes the modified polymer (a multi-vinylsulfone containing molecule), a multi-thiol containing molecule and a therapeutic molecule.
- the drug delivery system dissolves in water to form an aqueous solution, which undergoes gelatation upon administration to a site in a body.
- FIG. 1 is an example non-limiting process flow diagram of a method for generating a functional vinylsulfone group a hydroxyl-bearing molecule, according to an embodiment
- FIG. 2 is an example non-limiting process flow diagram of a method for controlling a number of vinylsulfone groups that are grafted on a hydroxyl-bearing polymer, according to an embodiment
- FIG. 3 is an example non-limiting process flow diagram of a nucleophile-Michael addition process, according to an embodiment
- FIG. 4 is an example non-limiting process flow diagram of a method for forming a hydrogel, according to an embodiment
- FIG. 5 is an example non-limiting process flow diagram of a method for administering a drug delivery system, according to an embodiment
- FIG. 6 is an example non-limiting process flow diagram of a method for forming a hydrogel encapsulating a therapeutic material at a site in the body, according to an embodiment
- FIG. 7 is an exemplary non-limiting illustration of results of 1H NMR confirming modification of hyaluranic acid with vinylsulfone, according to an embodiment
- FIG. 8 is an exemplary non-limiting illustration of results of 1H NMR confirming modification of dextran with vinylsulfone, according to an embodiment
- FIG. 9 is an exemplary non-limiting illustration of results of 1H NMR confirming modification of polyvinyl acetate with vinylsulfone, according to an embodiment
- FIG. 10 is an exemplary non-limiting illustration of results of 1H NMR confirming modification of algenate with vinylsulfone, according to an embodiment
- FIG. 11 is an exemplary non-limiting illustration of results of 1H NMR
- FIG. 12 is an exemplary non-limiting table illustrating the degree of modification of hyaluranic acid with vinylsulfone using different synthesis methods, according to an embodiment
- FIG. 13 is an exemplary non-limiting graph illustrating the degree of modification of dextran with vinylsulfone, according to an embodiment
- FIG. 14 shows exemplary non-limiting results of an assay showing that vinylsulfone-modified hyaluranic acid is not cytotoxic at various concentrations (0.1% to 1%) and different incubation times (5 hours and 20 hours), according to an embodiment
- FIG. 15 shows exemplary non-limiting gelatation kinetics and pictures of the actual gel, according to an embodiment
- FIG. 16 is an exemplary non-limiting illustration of results of 1H NMR
- FIG. 17 is an exemplary non-limiting binocular indirect microscope image of peripheral rabbit retina after intravitral injection of 10% hyaluranic acid, according to an embodiment
- FIG. 18 is an exemplary non-limiting graph showing the in vitro release of antibody from a hyaluranic acid hydrogel, according to an embodiment
- FIG. 19 is an exemplary non-limiting graph showing the in vitro release of antibody from a hyaluranic acid hydrogel, according to an embodiment
- FIG. 20 are exemplary non-limiting representative binocular indirect microscope images of the peripheral retina of the rabbit, showing no sign of hemorrhage, retinal detachment, edema, neovascularization, or other damage, according to an embodiment;
- FIG. 21 is an exemplary non-limiting illustration of sub-Tenon's injection of polymers into the rabbit eye, according to an embodiment
- FIG. 22 is an exemplary non-picture taken 1 week after intravitreal injection of
- FIG. 23 is an exemplary non-limiting comparison of the fluorescence in sclera and vitreous of treated and control eye, according to an embodiment.
- a multi-vinylsulfone molecule a multi hydroxyl-bearing water soluble molecule modified with two or more vinylsulfone groups.
- the multi-vinylsulfone containing molecule can be formed by dissolving a water soluble molecule containing a hydroxyl group in an aqueous solution to form a solution; adding a molecule containing two vinylsulfone groups to the solution; and forming a modified molecule by controlling a number of the vinylsulfone groups that are added to the molecule.
- the hydrogel includes the multi-vinylsulfone containing molecule and a multi-thiol containing molecule and can be formed from an aqueous solution that includes the multi-vinylsulfone containing molecule and the multi-thiol containing molecule that undergoes gelatation upon delivery to a site in the body.
- the multi-vinylsulfone containing molecule is active toward the multi-thiol containing molecule at mild aqueous conditions.
- Method 100 allows for simple, efficient and controllable modification of a hydroxyl-bearing molecule with a functional vinylsulfone group.
- Method 100 takes places an aqueous environment ("aqueous solution") to maximize the yield and/or minimize the potential hazard when the modified molecule is used in a biological system.
- a water soluble molecule containing a hydroxyl group is dissolved in an aqueous solution to form a solution.
- the aqueous solution in an embodiment, is an alkaline aqueous solution.
- the alkaline aqueous solution can have a pH greater than 7. In an embodiment, the alkaline aqueous solution has a pH from about 8 to about 15.
- the water soluble molecule containing the hydroxyl group is dissolved in the aqueous solution with a pH of about 7 and after the water soluble molecule containing the hydroxyl group is dissolved, the pH of the solution is adjusted to be alkaline.
- the aqueous solution can include a salt, an aqueous solvent, any other molecule that regulates the pH of the solution, any other molecule that facilitates the modification, or any other molecule that minimizes the potential hazard when the modified molecule is used in a biological system.
- the water soluble molecule containing a hydroxyl group is a water soluble polymer containing a hydroxyl group.
- a water soluble polymer containing a hydroxyl group include: hyaluranic acid (HA), polyethylene glycol (PEG), dextran, polyvinyl alcohol (PVA), alginate, cyclodextrin, and the like.
- the modification is a simple and efficient process.
- a molecule containing two vinylsulfone groups is added to the solution.
- An example of a molecule containing two vinylsulfone groups is divinylsulfone (DVS).
- a modified molecule is formed by controlling a number of the vinylsulfone groups that are added to the molecule.
- the modified molecule is formed by a one-step process using water as the solvent.
- a high pH alkaline, pH greater than about 7
- the dissolved molecule containing hydroxyl is reactive to the molecule containing at least two vinylsulfone groups.
- the vinylsulfone groups are added to the molecule when the dissolved molecule reacts with molar excess of the molecule containing two vinylsulfone groups.
- the modified molecule is biocompatible.
- the vinylsulfone groups grafted on the modified molecule are active and chemically reactive with a counterpart.
- the counterpart is a molecule containing a nucleophile.
- the vinylsulfone groups can covalently bond to the nucleophile.
- nucleophiles examples include thiols and amines.
- FIG. 2 illustrated is an example non-limiting process flow diagram of a method 200 for controlling a number of vinylsulfone groups that are grafted on a hydroxyl-bearing polymer, according to an embodiment.
- a water soluble polymer containing a hydroxyl group is dissolved in an aqueous solution to form a polymer solution.
- the water soluble polymer containing a hydroxyl group can be any polymer that is water soluble and contains one or more hydroxyl groups.
- Examples of a water soluble polymer containing a hydroxyl group include: hyaluranic acid (HA), polyethylene glycol (PEG), dextran, polyvinyl alcohol (PVA), alginate, cyclodextrin, and the like.
- HA hyaluranic acid
- PEG polyethylene glycol
- PVA polyvinyl alcohol
- a molecule containing two vinylsulfone groups is added to the polymer solution.
- An example of a molecule containing two vinylsulfone groups is
- the aqueous solution and/or the polymer solution is alkaline.
- the alkaline solution has a pH greater than about 7.
- the alkaline solution has a pH from about 8 to about 15.
- the alkaline solution has a pH from about 11.5 to about 16.
- the alkaline solution has a pH from about 11.5 to about 14.5.
- reaction conditions are varied to control a number of the vinylsulfone groups that are grafted on the polymer or a degree of modification of the polymer.
- the degree of modification can be controlled over a wide range. Examples of different mechanisms for controlling the number of vinylsulfone groups that are added to the molecule include: varying a reaction time, varying a reaction pH, varying an amount of molecules containing two vinylsulfone groups, varying a molar ratio between the vinylsulfone groups and the hydroxyl groups, varying a basicity of the aqueous solution, or the like.
- the modified polymer is formed.
- the water soluble molecule containing a hydroxyl group is hyaluranic acid.
- Hyaluranic acid is a polymer that contains four hydroxyl groups per
- Hyaluranic acid is reactive toward divinylsulfone at a high pH.
- hyaluranic acid is reactive toward divinylsulfone at a pH greater than about 11.5.
- hyaluranic acid is reactive toward divinylsulfone at a pH from about 12 to about 14.5. In another embodiment, hyaluranic acid is reactive toward divinylsulfone at a pH of about 13.3.
- the pKa of hydroxyl groups in saccharides is from about 12 to about 13.
- alkoxide ion in a high pH environment (greater than about 11.5), most of the hydroxyl groups are deprotonated and become an alkoxide ion (RO " ). Being an active nucleophile, the alkoxide ion can form a covalent linkage with the electrophilic double bond of vinylsulfone by 1 ,4- nucleophillic conjugate addition (Michael-type addition).
- the Michael-type addition reaction has been previously used to cross link hyaluranic acid with divinylsulfone.
- the molar ratio of divinylsulfone to hydroxyl is low (e.g., 1 :4), such that both vinylsulfone groups of each divinylsulfone react with hydroxyl groups of hyaluranic acid and crosslink the hyaluranic acid chains.
- Crosslinking can be avoided if the vinylsulfone groups of the divinylsulfone are in excess to the hydroxyl groups from the hyaluranic acid (the divinylsulfone to hydroxyl molar ratio is increased).
- the reaction can be further controlled by optimizing reaction parameters, including, for example, pH and time. The result is that divinylsulfone is not used as a crosslinker, but as a reagent to modify polymers by a simple "click" reaction.
- a “click” reaction is a reaction tailored to generate substances quickly and reliably by joining small (modular) units together.
- a “click” reaction is modular, is wide in scope, gives high chemical yields, generates inoffensive byproducts, is stereospecific, is physiologically stable, exhibits a large thermodynamic force (greater than about 84 kJ/mol) to favor a reaction with a single reaction product, and has a high atom economy.
- a "click” reaction has simple reaction conditions, uses readily available starting materials and reagents, uses no solvent or uses a solvent that is benign or easily removed (water), and provides simple product isolation by non-chromatographic means.
- the method for synthesizing the modified polymers is a simple
- the modified polymers instead of forming pre-crosslinked hydrogels, generate “clickable” precursors that are suitable for a wide range of biomedical uses. Examples of biomedical uses include drug delivery and tissue engineering.
- FIG. 3 illustrated is an example non-limiting process flow diagram of a nucleophile-Michael addition process 300, according to an embodiment.
- a multi-vinylsulfone containing molecule is formed.
- the multi-vinylsulfone containing molecule and a molecule containing a nucleophile are covalently bonded under mild physiological conditions.
- mild physiological conditions refer to a pH from about 5 to about 9, a temperature from about 10 to about 40 degrees Celsius, or a water content of at least about 90%.
- mild physiological conditions refer to a pH of about 7.4, a pressure of about 1 atm, a temperature of about 37 degrees Celsius, or a water content of at least about 99%.
- nucleophiles are amines and thiols.
- the multi-vinylsulfone containing molecule is a multi- vinylsulfone functionalized polymer and the nucleophile is a thiol.
- the multi-vinylsulfone functionalized polymer can participate in a subsequent thiol-Michael addition reaction with a thiol counterpart.
- the thiol-Michael addition reaction occurs between electrophilic double bonds and thiols.
- thiols are partially deprotonated and become thiol anions (S ⁇ Michael acceptors), which can readily react with certain electron-deficient double bonds, such as the double bonds of the vinylsulfone groups (Michael acceptor).
- S ⁇ Michael acceptors thiol anions
- the reaction between the vinylsulfone groups and the thiols is compatible to proteins, cells, and other biological structures.
- the click reaction between the vinylsulfone groups and the thiols is conducive to forming a hydrogel.
- the hydrogel includes the multi-vinylsulfone containing molecule and the multi-thiol containing molecule.
- FIG. 4 illustrated is a non-limiting process flow diagram of a method 400 for synthesizing a hydrogel.
- an aqueous solution of the multi-vinylsulfone containing molecule and the multi-thiol containing molecule is injected into a site in the body.
- the multi-vinylsulfone containing molecule can be a water soluble polymer containing hydroxyl groups modified with vinylsulfone functional groups according to methods 100 or 200 and the multi-thiol containing molecule containing thiol.
- the multi-thiol containing molecule is a polymer containing at least two thiol groups.
- the multi-vinylsulfone containing molecule and/or the multi- thiol containing molecule is a polysaccharide derivative.
- the hydrogel is formed at the site from the aqueous solution by covalently bonding the multi-vinylsulfone containing molecule and the multi-thiol containing molecule.
- the aqueous solution can also include free vinylsulfone groups and/or thiol groups that can interact with therapeutics or with biological tissue.
- the free vinylsulfone groups and/or thiol groups can be modulated by a modulator molecule.
- the aqueous solution in another embodiment, can also include a salt, an organic solvent, a therapeutic agent or a modulator molecule.
- the hydrogel can be used in many applications, including a drug delivery system.
- FIG. 5 is an example non-limiting process flow diagram of a method 500 for administering a drug delivery system, according to an embodiment.
- the drug delivery system of method 500 employs polymers that can undergo in situ gelatation after injection to the body.
- polymers that can undergo in situ gelatation upon injection in the body are a multi-vinylsulfone containing molecule and a multi-thiol containing molecule.
- the multi-vinylsulfone containing molecule can be derived from a water soluble hydroxyl containing material according to methods 100-300.
- the multi-vinylsulfone containing molecule and/or the multi-thiol containing molecule are polymers.
- the polymers can be polysaccharide derivatives.
- the drug delivery system also includes a therapeutic molecule ("drug").
- therapeutic molecules include: biomacromolecules (e.g., proteins, peptides, nucleic acids, aptamers, etc.), particulated small molecular drugs, or particles encapsulating the particulated small molecular drugs.
- the therapeutic molecules can any therapeutic molecule that can be used to treat a posterior eye condition, including age-related macular degeneration and diabetic retinopathy.
- the drug delivery system including the multi-vinylsulfone containing molecule and a multi-thiol containing molecule and the therapeutic molecule are dissolved in an aqueous buffer to form an aqueous solution.
- the aqueous buffer is water.
- the aqueous solution undergoes gelatation upon administration to a site in a body.
- the site in the body is a surface of the body or an interior of the body.
- the site is the posterior of the eye.
- the aqueous solution is administered to the site, in an embodiment, by injection.
- the aqueous solution can be easily injected to the site, even with a small needle, so that the therapeutic material can be placed at the targeted position with minimum impact on surrounding tissues.
- the injection can be an injection to the surface of the body or to an interior of the body.
- Example types of injection include: intravitrial injection, peribulbar injection, subtenon injection, or the like.
- the needle for the injection can be, for example, 31 gauged so that the therapeutics can be placed at a targeted position with minimum impact on the surrounding ocular tissues.
- the aqueous solution can undergo gelatation when the multi-vinylsulfone containing molecule forms a covalent bond with the multi-thiol containing molecule.
- the covalently bonded multi-thiol containing molecule and multi-vinylsulfone containing molecule can form a hydrogel according to method 400.
- the multi-vinylsulfone containing molecule and the multi-thiol containing molecule are crosslinked after injection into hydrophilic chains.
- the therapeutic molecule is encapsulated within a network formed by the multi-vinylsulfone containing molecule and the multi-thiol containing molecule.
- the crosslinked network protects the therapeutic molecule from digestion by enzymes and avoids the therapeutic molecule contacting tissues.
- different types of therapeutic materials for example, biomacromolecule and small molecule encapsulated particles
- the hydrogel has an aqueous environment inside.
- aqueous environment inside the hydrogel versus a hydrophobic environment inside a traditional polymer implant enables the labile biomolecules to maintain correct three-dimensional structure and enhances stability of the labile biomolecules and helps to maintain therapeutic efficacy of the labile biomolecules.
- drug encapsulating particles after being encapsulated in the hydrogel, will not contact the blood/lymphatic system, reducing the chance of being eliminated. In the eye, this encapsulation also reduces the risk of elicit adverse effects, such as sterile endophalmitis by contacting ocular tissue.
- mild physiological conditions refer to a pH from about 5 to about 9, a temperature from about 10 to about 40 degrees Celsius, or a water content of at least about 90%.
- mild physiological conditions refer to a pH of about 7.4, a pressure of about 1 atm, a temperature of about 37 degrees Celsius, or a water content of at least about 99%.
- the hydrogel drug delivery system can facilitate controlled drug delivery to the site.
- the hydrogel drug delivery system is useful for prolonged delivery of therapeutics to the site. Therapeutics can be delivered to the site for days, months or years.
- the release rate of the therapeutic molecule can be controlled, for example, by controlling the crosslinking density. Additionally, the release rate can be further controlled by selecting different polymers for the release of different drugs. For example, when long term release is desirable, a positively charged drug, like Avastin, can be better trapped in a negatively charged polymer, like multi-vinylsulfone hyaluranic acid.
- Method 600 refers to an in situ forming hydrogel formulation for controlled delivery of therapeutics to a site in the body.
- the therapeutics are macromolecule and/or small molecular therapeutics and the site the body is the eye.
- components are dissolved and mixed in an aqueous solution.
- the components include polymers with multiple vinylsulfone groups per molecule formed according to methods 100-300, molecules having multiple thiols per molecule, and therapeutic molecules and/or therapeutic molecule-encapsulated particles.
- the aqueous solution with the mixed components is injected to a site in the body.
- the site in the body is the eye.
- the polymers with multiple vinylsulfone groups per molecule formed according to methods 100-300 and the molecules having multiple thiols per molecule are crosslinked and the therapeutic material is encapsulated within the crosslinked network at mild physiological conditions.
- a hydrogel is formed that encapsulates the therapeutic material with a controlled gelatation time.
- the formation and encapsulation are each in situ processes.
- the gelatation time is well controlled so that the hydrogel is completely formed shortly after injection, but not too fast to allow manipulation of the therapeutic material.
- the gelatation time sufficient to allow complete encapsulation of the therapeutic material, but shorter than a time of elimination of the free therapeutic material via circulation of the blood or lymph.
- the following examples illustrate modification of hyaluranic acid, dextran, polyvinyl alcohol, alginate and polyethylene glycol with vinylsulfone groups.
- the methods 100-600 are not limited to merely these polymers; instead, methods 100-600 are applicable to all hydroxyl containing water soluble polymers.
- the values of reaction variables, such as, the concentration of the polymers, pH, vinylsulfone to hydroxide ratio, and the like, and/or the protocols of the method, such as, the purification procedure, choice of polymer, choice of thiol containing molecules, reaction time, reaction buffer, and the like can be changed to control the addition of vinylsulfone groups to the polymers in the formation of the modified polymers.
- the vinylsulfone groups of the modified polymers can participate in a subsequent thiol-Michael "click" reaction with a thiol counterpart.
- Hyaluranic acid was dissolved in 0.1 M NaOH at 2% w/v (corresponding to approximately 200 ⁇ hydroxyl groups per ml). Divinylsulfone was added into a vigorously vortexing hyaluranic acid solution in excess at a molar ratio of 1.25-times the hydroxyl groups of hyaluranic acid. The reaction was carried out for 10 minutes and stopped by adjusting the pH to 5 using 5M HC1. After adjusting the pH, the solution was purified by dialysis and freeze-dried. [0072] The success of conjugation was confirmed by 1H NMR, as shown in FIG. 7. FIG.
- FIG. 7(A) relates to unmodified hyaluranic acid and FIG. 7(B) relates to hyaluranic acid modified with vinylsulfone.
- Element 702 is an illustration of the chemical structure of unmodified hyaluranic acid and element 704 is an illustration of the chemical structure of hyaluranic acid modified with vinylsulfone.
- Element 706 is the 1H NMR spectrum of unmodified hyaluranic acid and element 708 is the 1H NMR spectrum of hyaluranic acid modified with vinylsulfone.
- the degree of modification of a certain hydroxyl containing water soluble polymer can be controlled by at least three factors: reaction pH, reaction time and the molar ratio between divinylsulfone and OH.
- a hyaluranic acid solution was dissolved in nanopure water ® and adjusted to different pH values (in the range of 9 to 10) by drop- wise addition of 6 M NaOH.
- Divinylsulfone was added into the vigorously vortexing hyaluranic acid solution, at a molar ratio of 1.25-times in excess of the hydroxyl groups of hyaluranic acid.
- the reaction was carried out for 12 hours and stopped by adjusting the pH to 5 using 5M HC1.
- HA was dissolved in 0.01 M or 0.1 M NaOH solution at 2% w/v.
- Divinylsulfone was added into the vigorously vortexing hyaluranic acid solution at a molar ratio of 1.25-times the hydroxyl groups of hyaluranic acid.
- the reactions were stopped at predetermined time points by adjusting the pH to 5 using 5M HCl.
- hyaluranic acid was dissolved in 0.1 M NaOH and divinylsulfone was added instantly into the vigorously vortexing hyaluranic acid solution at a molar ratio of 1.25, 2.5, or 10 times the hydroxyl groups of hyaluranic acid.
- the reactions were stopped at pre-determined time points by adjusting the pH to 5 using 5M HCl. After the pH adjustment, the solution was purified by diafiltration and freeze-dried.
- predetermined time points by adjusting the pH to 5 using 5M HCl. After the pH adjustment, the solution was purified by dialysis or diafiltration or other types of methods and freeze-dried. The success of conjugation and the DM was examined by 1H NMR, as illustrated in FIG . 13.
- NIH 3T3 cells were cultured on a 96 well plate, and vinylsulfone-modified hyaluranic acid of concentration 0.1% to 1% was added to the cell and incubated for 5 hours or 20 hours before the assays were performed. As shown in FIG. 14, no cytotoxic effect were observed (in the assays, live cells appear green and dead cells appear red; no red was observed). Reaction of vinylsulfone-modified polymers with thiols
- the vinylsulfone modified polymers can react with thiol at mild aqueous conditions. Since these conditions are compatible with labile biomolecules, cells, animals and humans, the vinylsulfone modified polymers are excellent materials for preparing in situ hydrogel, polymer-drug conjugate, protein encapsulation, surface modification, or the like.
- Vinylsulfone-modified hyaluranic acid was dissolved in an aqueous buffer solution, for example 0.1M, pH 7.4 phosphate buffer (PB), at various concentrations, at 7% w/v.
- Dithiolthreitol which is a small molecules containing two thiols was dissolved in the same buffer solution at O.lmg/ ⁇ and added to the polymer solution at the molar ratio of 1 :1/SH:VS.
- the gelatation kinetics 1504 and pictures of the actual gel 1502 are shown in FIG. 15.
- Vinylsulfone-modified dextran was dissolved in an aqueous buffer solution, for example 0.1M pH 7.4 phosphate buffer (PB), at various concentrations at 7% w/v.
- PB pH 7.4 phosphate buffer
- the crosslinker dithiothreitol was dissolved in the same buffer solution at O.lmg/ ⁇ and added to the polymer solution at the molar ratio of 1 :1/SH:VS.
- the gelatation kinetics 1506 and pictures of the actual gel 1508 are shown in FIG. 15.
- Vinylsulfone-modified dextran was dissolved an aqueous buffer solution, for example, 0.1M pH 7.4 PB, at 1% w/v.
- Two-time excessive (molar ratio to vinylsulfone group) glutathione was added to polymer solution. The reaction was carried out for 2 hours at room temperature and the produced was thoroughly dialysis and freeze dried. The success of conjugation was examined by 1H NMR, as shown in FIG. 16, element 1604.
- vinylsulfone grafted hyaluranic acid was used as an example. Vinylsulfone grafted hyaluranic acid was dissolved in PBS at 10% w/v and injected to the rabbit eye by intravitreal injection. The retina of the rabbit was examined using binocular indirect microscope (BIO).
- FIG. 17 shows a representative binocular indirect microscope image.
- Polymers having two or more vinylsulfone groups per each molecule can be crosslinked by small molecules having two or more thiols.
- the following are examples of two vinylsulfone grafted polymers, vinylsulfone grafted hyaluranic acid and vinylsulfone grafted dextran crosslinked by a small dithiol molecule dithiothreitol at physiological pH.
- this method is not limited to these two polymers and the particular crosslinking molecules we used, and the detail protocol used, for example the specific buffer, pH, concentration, purification method , and the like, are merely examples.
- Vinylsulfone grafted hyaluranic acid was dissolved in an aqueous buffer solution, for example 0.1M pH 7.4 phosphate buffer saline (PBS), at various concentrations.
- PBS phosphate buffer saline
- Dithiolthreitol which is a small molecules containing two thiols was dissolved in the same buffer solution at O.lmg/ ⁇ and added to the polymer solution at the molar ratio of
- a hydrogel is formed shortly after mixing.
- Vinylsulfone grafted dextran was dissolved in an aqueous buffer solution, for example PBS, at various concentrations.
- the crosslinker dithiothreitol was dissolved in the same buffer solution at 0. lmg/ ⁇ and added to the polymer solution at the molar ratio of 1 : 1/SH:VS.
- a hydrogel was formed shortly after mixing.
- Polymers having two or more vinylsulfone groups per each molecule can be crosslinked by another large molecule, for example polymers, having two or more thiols per molecule.
- reaction was carried out for 30 minutes, stopped by readjusting pH to 4.5 by 1M HC1, and purified by diafiltration and freeze dried. The success of modification was monitored by the elimination of vinylsulfone double bond from ⁇ NMR spectrum and Ellman's assay.
- Vinylsulfone grafted hyaluronic acid and HA-SH were dissolved separately in an aqueous buffer solution, for example PBS, at various concentrations, for example 10% w/v.
- Vinylsulfone grafted dextran and dextran-SH were dissolved separately in an aqueous buffer solution, for example PBS, at various concentrations, for example 10% w/v.
- hydrogel formed shortly Reaction of vinylsulfone grafted dextran with HA-SH and the preparation of in situ hydrogel
- Vinylsulfone grafted dextran and HA-SH were dissolved separately in an aqueous buffer solution, for example PBS, at various concentrations, for example 10% w/v. Upon mixing, a hydrogel formed shortly
- a hyaluronic acid based hydrogel either composed of vinylsulfone grafted hyaluronic acid crosslinked by small molecule crosslinker dithiothreitol or polymer crosslinker HA-SH, and three model proteins bovine serum albumin (BSA), near infrared labeled IgG (NIR-IgG) and Avastin, were used as a model polymer and macromolecule.
- BSA bovine serum albumin
- NIR-IgG near infrared labeled IgG
- Avastin Avastin
- Avastin is a full length antibody drug widely used for treating various eye diseases, including age-related macular degeneration.
- Avastint has molecular weight of 150 kDa and is positively charged at a neutral pH.
- a negatively charged polymer hyaluranic acid can be used to prolong the release of the drug.
- Hydrogel made from vinylsulfone grafted hyaluronic acid crosslinked with dithiothreitol and the release of BSA
- BSA was dissolved in a pH 7.4 buffer solution, at various concentration from 0.1% to 10% w/v.
- vinylsulfone grafted hyaluranic acid was dissolved in this protein solution.
- the crosslinker dithiothreitol was dissolved in the same buffer solution at O.lmg/ ⁇ and added to the vinylsulfone grafted hyaluranic acid/BSA solution at the molar ratio of 1 :1/SH:VS.
- Gel was formed after mixing, and the protein was encapsulated in the gel. PBS was then added as sink for the protein to release. Protein (BSA) release data for more than two months was shown in FIG. 18. Less than 30% of the protein was released.
- Hydrogel made from vinylsulfone grafted hyaluronic acid crosslinked with HASH and the release ofNIR-IgG and Avastin
- the following example shows how to encapsulate drug-encapsulated particles in the in situ hydrogel.
- the model drug molecule used is triamcinolone, a steroid drug widely used for treating various ocular inflammation.
- Model drug triamcinolone can be encapsulated in two component nanoparticles form by FTAEA and F-moc phenylalanine of diameter about 100 nm. The particles are dissolved in a pH 7.4 buffer solution.
- Vinylsulfone grafted hyaluranic acid is dissolved a pH 7.4 buffer solution and mixed with the nanoparticle solution.
- HA-SH dissolved in the same buffer solution as vinylsulfone grafted hyaluranic acid is added to vinylsulfone grafted hyaluranic acid
- FIG. 22 is a picture of the bisected rabbit eye ball. A transparent hydrogel is clearly seen surrounded by the vitreous.
- FIG. 23 shows the comparison of vitreous from treated eye and control eye.
- the fluorescence in the vitreous of treated eye indicates the release of drug in vivo.
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Abstract
A multi-vinylsulfone containing molecule is described herein. The multi-vinylsulfone containing molecule can be formed by dissolving a water soluble polymer containing a hydroxyl group in an aqueous solution to form a polymer solution; adding a molecule containing two vinylsulfone groups to the polymer solution; and forming a modified polymer by controlling a number of the vinylsulfone groups that are added to the polymer. A hydrogel is also described herein that can include the multi-vinylsulfone containing molecule and a multi-thiol containing molecule. The hydrogel can be formed from an aqueous solution that includes the multi-vinylsulfone containing molecule and the multi-thiol containing molecule by undergoing gelatation upon delivery to a site in the body. Also described is a drug delivery system that employs the hydrogel.
Description
MULTI-VINYLSULFONE CONTAINING MOLECULE
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application claims priority to US provisional application number 61/457,836, entitled: "A method for generating vinylsulfone group on hydroxyl bearing water soluble polymer," and filed on June 13, 2011. This application also claims priority to US provisional application number 61/457,837, entitled: "In situ hydrogel delivery system for treating posterior eye conditions," and filed on June 13, 2011.
TECHNICAL FIELD
[0002] This disclosure generally relates to generation of a multi-vinylsulfone molecule and to applications of the multi-vinylsulfone containing molecule.
BACKGROUND
[0003] Many polymers used in biomedical applications are hydroxyl-bearing water soluble polymers. Examples of hydroxyl-bearing water soluble polymers include: hyaluranic acid (HA), polyethylene glycol (PEG), dextran, polyvinyl alcohol, alginate, cyclodextrin, and the like. Hydroxyl-bearing water soluble polymers are generally non-toxic, and the hydroxyl groups generally allow these polymers to be soluble in an aqueous environment. However, hydroxyl- bearing water soluble polymers alone do not usually have functionality toward animal cells or tissues and must be modified with an active agent to exhibit functionality toward animal cells or tissues.
[0004] For example, hydroxyl-bearing water soluble polymers can be linked with hydrophobic anti-cancer drugs to increase the solubility and targeting of the anticancer drug. Hydroxyl-bearing water soluble polymers can be linked with proteins or other labile
biomolecules to increase the half life of a drug in circulation. Other examples include making nanoparticles and imaging agents. The hydroxyl-bearing water soluble polymer can also be modified for use as a hydrogel. A hydrogel made with a modified hydroxyl-bearing water soluble polymer can be used, for example, in a tissue engineering scaffold, a drug delivery depot, a drug carrier in polymer-drug conjugates, as well as other biomedical applications. Modifying
hydroxyl-bearing water soluble polymers for use in a hydrogel traditionally involves complicated chemistry and harsh conditions, which may be expensive and not suitable for biomedical applications.
[0005] The above-described background is merely intended to provide an overview of contextual information regarding hydroxyl-bearing water soluble polymers, and is not intended to be exhaustive. Additional context may become apparent upon review of one or more of the various non-limiting embodiments of the following detailed description.
SUMMARY
[0006] The following presents a simplified summary of the specification in order to provide a basic understanding of some aspects of the specification. This summary is not an extensive overview of the specification. It is intended to neither identify key or critical elements of the specification nor delineate any scope of particular embodiments of the specification, or any scope of the claims. Its sole purpose is to present some concepts of the specification in a simplified form as a prelude to the more detailed description that is presented later.
[0007] In accordance with one or more embodiments and corresponding disclosure, various non-limiting aspects are described in connection with a hydroxyl-bearing water soluble polymer modified with two or more vinylsulfone groups. The modified polymer can be combined with an active agent and/or form crosslinks between polymers at in aqueous medium at mild physiological conditions of a pH of about 7.4, a pressure of about 1 atm, or a temperature of about 37 degrees Celsius.
[0008] A method of forming the modified polymer is described, according to an embodiment. A water soluble polymer containing a hydroxyl group is dissolved in an aqueous solution to form a polymer solution. A molecule containing two vinylsulfone groups is added to the polymer solution. The modified polymer is formed by controlling a number of the vinylsulfone groups that are grafted to the polymer. The vinylsulfone groups are chemically reactive.
[0009] According to another embodiment, a hydrogel that can be made from the modified polymer is described. The hydrogel includes the modified polymer (a multi- vinylsulfone containing molecule) and a multi-thiol containing molecule. The hydrogel is formed at a site of a biological tissue upon delivery to the site. The hydrogel is formed from an aqueous
solution that includes the modified polymer and the multi-thiol containing molecule by a covalent bond between the modified polymer and the multi-thiol containing molecule.
[0010] In a further embodiment, a drug delivery system is described. The drug delivery system includes the modified polymer (a multi-vinylsulfone containing molecule), a multi-thiol containing molecule and a therapeutic molecule. The drug delivery system dissolves in water to form an aqueous solution, which undergoes gelatation upon administration to a site in a body.
[0011] The following description and the drawings set forth certain illustrative aspects of the specification. These aspects are indicative, however, of but a few of the various ways in which the various embodiments of the specification may be employed. Other aspects of the specification will become apparent from the following detailed description of the specification when considered in conjunction with the drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
[0012] Numerous aspects and embodiments are set forth in the following detailed description, taken in conjunction with the accompanying drawings, in which like reference characters refer to like parts throughout, and in which:
[0013] FIG. 1 is an example non-limiting process flow diagram of a method for generating a functional vinylsulfone group a hydroxyl-bearing molecule, according to an embodiment;
[0014] FIG. 2 is an example non-limiting process flow diagram of a method for controlling a number of vinylsulfone groups that are grafted on a hydroxyl-bearing polymer, according to an embodiment;
[0015] FIG. 3 is an example non-limiting process flow diagram of a nucleophile-Michael addition process, according to an embodiment;
[0016] FIG. 4 is an example non-limiting process flow diagram of a method for forming a hydrogel, according to an embodiment;
[0017] FIG. 5 is an example non-limiting process flow diagram of a method for administering a drug delivery system, according to an embodiment;
[0018] FIG. 6 is an example non-limiting process flow diagram of a method for forming a hydrogel encapsulating a therapeutic material at a site in the body, according to an embodiment;
[0019] FIG. 7 is an exemplary non-limiting illustration of results of 1H NMR confirming modification of hyaluranic acid with vinylsulfone, according to an embodiment;
[0020] FIG. 8 is an exemplary non-limiting illustration of results of 1H NMR confirming modification of dextran with vinylsulfone, according to an embodiment;
[0021] FIG. 9 is an exemplary non-limiting illustration of results of 1H NMR confirming modification of polyvinyl acetate with vinylsulfone, according to an embodiment;
[0022] FIG. 10 is an exemplary non-limiting illustration of results of 1H NMR confirming modification of algenate with vinylsulfone, according to an embodiment;
[0023] FIG. 11 is an exemplary non-limiting illustration of results of 1H NMR
confirming modification of polyethylene glycol with vinylsulfone , according to an embodiment;
[0024] FIG. 12 is an exemplary non-limiting table illustrating the degree of modification of hyaluranic acid with vinylsulfone using different synthesis methods, according to an embodiment;
[0025] FIG. 13 is an exemplary non-limiting graph illustrating the degree of modification of dextran with vinylsulfone, according to an embodiment;
[0026] FIG. 14 shows exemplary non-limiting results of an assay showing that vinylsulfone-modified hyaluranic acid is not cytotoxic at various concentrations (0.1% to 1%) and different incubation times (5 hours and 20 hours), according to an embodiment;
[0027] FIG. 15 shows exemplary non-limiting gelatation kinetics and pictures of the actual gel, according to an embodiment;
[0028] FIG. 16 is an exemplary non-limiting illustration of results of 1H NMR
confirming the success of conjugation, according to an embodiment;
[0029] FIG. 17 is an exemplary non-limiting binocular indirect microscope image of peripheral rabbit retina after intravitral injection of 10% hyaluranic acid, according to an embodiment;
[0030] FIG. 18 is an exemplary non-limiting graph showing the in vitro release of antibody from a hyaluranic acid hydrogel, according to an embodiment;
[0031] FIG. 19 is an exemplary non-limiting graph showing the in vitro release of antibody from a hyaluranic acid hydrogel, according to an embodiment;
[0032] FIG. 20 are exemplary non-limiting representative binocular indirect microscope images of the peripheral retina of the rabbit, showing no sign of hemorrhage, retinal detachment, edema, neovascularization, or other damage, according to an embodiment;
[0033] FIG. 21 is an exemplary non-limiting illustration of sub-Tenon's injection of polymers into the rabbit eye, according to an embodiment;
[0034] FIG. 22 is an exemplary non-picture taken 1 week after intravitreal injection of
NR-IgG encapsulated hydrogel with the arrow indicating the location of the hydrogel, according to an embodiment; and
[0035] FIG. 23 is an exemplary non-limiting comparison of the fluorescence in sclera and vitreous of treated and control eye, according to an embodiment.
DETAILED DESCRIPTION
[0036] Various aspects or features of this disclosure are described with reference to the drawings, wherein like reference numerals are used to refer to like elements throughout. In this specification, numerous specific details are set forth in order to provide a thorough understanding of this disclosure. It should be understood, however, that the certain aspects of disclosure may be practiced without these specific details, or with other methods, components, molecules, etc. In other instances, well-known structures and devices are shown in block diagram form to facilitate description and illustration of the various embodiments.
[0037] In accordance with one or more embodiments described in this disclosure, described herein is a multi-vinylsulfone molecule: a multi hydroxyl-bearing water soluble molecule modified with two or more vinylsulfone groups. The multi-vinylsulfone containing molecule can be formed by dissolving a water soluble molecule containing a hydroxyl group in an aqueous solution to form a solution; adding a molecule containing two vinylsulfone groups to the solution; and forming a modified molecule by controlling a number of the vinylsulfone groups that are added to the molecule. Also described are applications of the multi-vinylsulfone containing molecule, including a hydrogel and a drug delivery system employing the hydrogel. The hydrogel includes the multi-vinylsulfone containing molecule and a multi-thiol containing molecule and can be formed from an aqueous solution that includes the multi-vinylsulfone containing molecule and the multi-thiol containing molecule that undergoes gelatation upon
delivery to a site in the body. The multi-vinylsulfone containing molecule is active toward the multi-thiol containing molecule at mild aqueous conditions.
[0038] Referring now to the drawings, with reference initially to FIG. 1 , illustrated is an example non-limiting process flow diagram of a method 100 for generating a functional vinylsulfone group a hydroxyl-bearing molecule, according to an embodiment. Method 100 allows for simple, efficient and controllable modification of a hydroxyl-bearing molecule with a functional vinylsulfone group.
[0039] Method 100 takes places an aqueous environment ("aqueous solution") to maximize the yield and/or minimize the potential hazard when the modified molecule is used in a biological system. At element 102, a water soluble molecule containing a hydroxyl group is dissolved in an aqueous solution to form a solution. The aqueous solution, in an embodiment, is an alkaline aqueous solution. The alkaline aqueous solution can have a pH greater than 7. In an embodiment, the alkaline aqueous solution has a pH from about 8 to about 15. According to another embodiment, the water soluble molecule containing the hydroxyl group is dissolved in the aqueous solution with a pH of about 7 and after the water soluble molecule containing the hydroxyl group is dissolved, the pH of the solution is adjusted to be alkaline.
[0040] The aqueous solution can include a salt, an aqueous solvent, any other molecule that regulates the pH of the solution, any other molecule that facilitates the modification, or any other molecule that minimizes the potential hazard when the modified molecule is used in a biological system.
[0041] According to an embodiment, the water soluble molecule containing a hydroxyl group is a water soluble polymer containing a hydroxyl group. Examples of a water soluble polymer containing a hydroxyl group (or hydroxyl-containing water soluble polymers) include: hyaluranic acid (HA), polyethylene glycol (PEG), dextran, polyvinyl alcohol (PVA), alginate, cyclodextrin, and the like.
[0042] The modification is a simple and efficient process. At element 104, a molecule containing two vinylsulfone groups is added to the solution. An example of a molecule containing two vinylsulfone groups is divinylsulfone (DVS). At element 106, a modified molecule is formed by controlling a number of the vinylsulfone groups that are added to the molecule. The modified molecule is formed by a one-step process using water as the solvent. At a high pH (alkaline, pH greater than about 7), the dissolved molecule containing hydroxyl is
reactive to the molecule containing at least two vinylsulfone groups. The vinylsulfone groups are added to the molecule when the dissolved molecule reacts with molar excess of the molecule containing two vinylsulfone groups. In an embodiment, the modified molecule is biocompatible.
[0043] The vinylsulfone groups grafted on the modified molecule are active and chemically reactive with a counterpart. In an embodiment, the counterpart is a molecule containing a nucleophile. The vinylsulfone groups can covalently bond to the nucleophile.
Examples of nucleophiles include thiols and amines.
[0044] Referring now to FIG. 2, illustrated is an example non-limiting process flow diagram of a method 200 for controlling a number of vinylsulfone groups that are grafted on a hydroxyl-bearing polymer, according to an embodiment. At element 202, a water soluble polymer containing a hydroxyl group is dissolved in an aqueous solution to form a polymer solution. The water soluble polymer containing a hydroxyl group can be any polymer that is water soluble and contains one or more hydroxyl groups. Examples of a water soluble polymer containing a hydroxyl group include: hyaluranic acid (HA), polyethylene glycol (PEG), dextran, polyvinyl alcohol (PVA), alginate, cyclodextrin, and the like.
[0045] At element 204, a molecule containing two vinylsulfone groups is added to the polymer solution. An example of a molecule containing two vinylsulfone groups is
divinylsulfone. The aqueous solution and/or the polymer solution is alkaline. According to an embodiment, the alkaline solution has a pH greater than about 7. In another embodiment, the alkaline solution has a pH from about 8 to about 15. According to a further embodiment, the alkaline solution has a pH from about 11.5 to about 16. In another embodiment, the alkaline solution has a pH from about 11.5 to about 14.5.
[0046] At element 206, reaction conditions are varied to control a number of the vinylsulfone groups that are grafted on the polymer or a degree of modification of the polymer. According to an embodiment, the degree of modification can be controlled over a wide range. Examples of different mechanisms for controlling the number of vinylsulfone groups that are added to the molecule include: varying a reaction time, varying a reaction pH, varying an amount of molecules containing two vinylsulfone groups, varying a molar ratio between the vinylsulfone groups and the hydroxyl groups, varying a basicity of the aqueous solution, or the like. At element 208, the modified polymer is formed.
[0047] In an embodiment, the water soluble molecule containing a hydroxyl group is hyaluranic acid. Hyaluranic acid is a polymer that contains four hydroxyl groups per
disaccharide unit. Hyaluranic acid is reactive toward divinylsulfone at a high pH. For example, hyaluranic acid is reactive toward divinylsulfone at a pH greater than about 11.5. In an
embodiment, hyaluranic acid is reactive toward divinylsulfone at a pH from about 12 to about 14.5. In another embodiment, hyaluranic acid is reactive toward divinylsulfone at a pH of about 13.3.
[0048] The pKa of hydroxyl groups in saccharides is from about 12 to about 13.
Accordingly, in a high pH environment (greater than about 11.5), most of the hydroxyl groups are deprotonated and become an alkoxide ion (RO"). Being an active nucleophile, the alkoxide ion can form a covalent linkage with the electrophilic double bond of vinylsulfone by 1 ,4- nucleophillic conjugate addition (Michael-type addition).
[0049] The Michael-type addition reaction has been previously used to cross link hyaluranic acid with divinylsulfone. In cross linking, the molar ratio of divinylsulfone to hydroxyl is low (e.g., 1 :4), such that both vinylsulfone groups of each divinylsulfone react with hydroxyl groups of hyaluranic acid and crosslink the hyaluranic acid chains. Crosslinking can be avoided if the vinylsulfone groups of the divinylsulfone are in excess to the hydroxyl groups from the hyaluranic acid (the divinylsulfone to hydroxyl molar ratio is increased). The reaction can be further controlled by optimizing reaction parameters, including, for example, pH and time. The result is that divinylsulfone is not used as a crosslinker, but as a reagent to modify polymers by a simple "click" reaction.
[0050] Stoichiometrically, only one vinylsulfone group of each divinylsulfone molecule will react with the OH group of the hyaluranic acid. The other vinylsulfone group will remain unreacted. The remaining vinylsulfone groups can be used, for example, as in situ crosslinking points or protein conjugation points in a subsequent "click" reaction.
[0051] A "click" reaction is a reaction tailored to generate substances quickly and reliably by joining small (modular) units together. A "click" reaction is modular, is wide in scope, gives high chemical yields, generates inoffensive byproducts, is stereospecific, is physiologically stable, exhibits a large thermodynamic force (greater than about 84 kJ/mol) to favor a reaction with a single reaction product, and has a high atom economy. Preferably, a "click" reaction has simple reaction conditions, uses readily available starting materials and reagents, uses no solvent
or uses a solvent that is benign or easily removed (water), and provides simple product isolation by non-chromatographic means.
[0052] Additionally, the method for synthesizing the modified polymers is a simple
"click" method. This simple "click" method enables the modified polymers to become
"clickable" subsequently under physiological conditions. The modified polymers, instead of forming pre-crosslinked hydrogels, generate "clickable" precursors that are suitable for a wide range of biomedical uses. Examples of biomedical uses include drug delivery and tissue engineering.
[0053] Referring now to FIG. 3, illustrated is an example non-limiting process flow diagram of a nucleophile-Michael addition process 300, according to an embodiment. At element 302, a multi-vinylsulfone containing molecule is formed. At element 304, the multi-vinylsulfone containing molecule and a molecule containing a nucleophile are covalently bonded under mild physiological conditions. In an embodiment, mild physiological conditions refer to a pH from about 5 to about 9, a temperature from about 10 to about 40 degrees Celsius, or a water content of at least about 90%. In another embodiment, mild physiological conditions refer to a pH of about 7.4, a pressure of about 1 atm, a temperature of about 37 degrees Celsius, or a water content of at least about 99%. Examples of nucleophiles are amines and thiols.
[0054] In an embodiment, the multi-vinylsulfone containing molecule is a multi- vinylsulfone functionalized polymer and the nucleophile is a thiol. The multi-vinylsulfone functionalized polymer can participate in a subsequent thiol-Michael addition reaction with a thiol counterpart. The thiol-Michael addition reaction occurs between electrophilic double bonds and thiols. At physiological pH, thiols are partially deprotonated and become thiol anions (S\ Michael acceptors), which can readily react with certain electron-deficient double bonds, such as the double bonds of the vinylsulfone groups (Michael acceptor). The reaction between the vinylsulfone groups and the thiols is compatible to proteins, cells, and other biological structures.
[0055] The click reaction between the vinylsulfone groups and the thiols is conducive to forming a hydrogel. The hydrogel includes the multi-vinylsulfone containing molecule and the multi-thiol containing molecule. Referring now to FIG. 4, illustrated is a non-limiting process flow diagram of a method 400 for synthesizing a hydrogel. At element 402, an aqueous solution of the multi-vinylsulfone containing molecule and the multi-thiol containing molecule is injected into a site in the body. The multi-vinylsulfone containing molecule can be a water soluble
polymer containing hydroxyl groups modified with vinylsulfone functional groups according to methods 100 or 200 and the multi-thiol containing molecule containing thiol. According to an embodiment, the multi-thiol containing molecule is a polymer containing at least two thiol groups. In a further embodiment, the multi-vinylsulfone containing molecule and/or the multi- thiol containing molecule is a polysaccharide derivative.
[0056] At element 404, the hydrogel is formed at the site from the aqueous solution by covalently bonding the multi-vinylsulfone containing molecule and the multi-thiol containing molecule. The aqueous solution can also include free vinylsulfone groups and/or thiol groups that can interact with therapeutics or with biological tissue. The free vinylsulfone groups and/or thiol groups can be modulated by a modulator molecule. The aqueous solution, in another embodiment, can also include a salt, an organic solvent, a therapeutic agent or a modulator molecule.
[0057] The hydrogel can be used in many applications, including a drug delivery system.
FIG. 5 is an example non-limiting process flow diagram of a method 500 for administering a drug delivery system, according to an embodiment. The drug delivery system of method 500 employs polymers that can undergo in situ gelatation after injection to the body. Examples of polymers that can undergo in situ gelatation upon injection in the body are a multi-vinylsulfone containing molecule and a multi-thiol containing molecule. The multi-vinylsulfone containing molecule can be derived from a water soluble hydroxyl containing material according to methods 100-300. In an embodiment, the multi-vinylsulfone containing molecule and/or the multi-thiol containing molecule are polymers. The polymers can be polysaccharide derivatives.
[0058] The drug delivery system also includes a therapeutic molecule ("drug").
Examples of therapeutic molecules include: biomacromolecules (e.g., proteins, peptides, nucleic acids, aptamers, etc.), particulated small molecular drugs, or particles encapsulating the particulated small molecular drugs. In an embodiment, the therapeutic molecules can any therapeutic molecule that can be used to treat a posterior eye condition, including age-related macular degeneration and diabetic retinopathy.
[0059] According to method 500, at element 502, the drug delivery system, including the multi-vinylsulfone containing molecule and a multi-thiol containing molecule and the therapeutic molecule are dissolved in an aqueous buffer to form an aqueous solution. In an embodiment, the aqueous buffer is water. At element 504, the aqueous solution undergoes gelatation upon
administration to a site in a body. In an embodiment, the site in the body is a surface of the body or an interior of the body. In a further embodiment, the site is the posterior of the eye.
[0060] The aqueous solution is administered to the site, in an embodiment, by injection.
The aqueous solution can be easily injected to the site, even with a small needle, so that the therapeutic material can be placed at the targeted position with minimum impact on surrounding tissues. The injection can be an injection to the surface of the body or to an interior of the body. Example types of injection include: intravitrial injection, peribulbar injection, subtenon injection, or the like. When the site is the eye, the needle for the injection can be, for example, 31 gauged so that the therapeutics can be placed at a targeted position with minimum impact on the surrounding ocular tissues.
[0061] The aqueous solution can undergo gelatation when the multi-vinylsulfone containing molecule forms a covalent bond with the multi-thiol containing molecule. The covalently bonded multi-thiol containing molecule and multi-vinylsulfone containing molecule can form a hydrogel according to method 400.
[0062] The multi-vinylsulfone containing molecule and the multi-thiol containing molecule are crosslinked after injection into hydrophilic chains. The crosslinked hydrophilic chains and encapsulate the therapeutic molecule. The therapeutic molecule is encapsulated within a network formed by the multi-vinylsulfone containing molecule and the multi-thiol containing molecule. The crosslinked network protects the therapeutic molecule from digestion by enzymes and avoids the therapeutic molecule contacting tissues. Moreover, according to an embodiment, different types of therapeutic materials (for example, biomacromolecule and small molecule encapsulated particles) can be encapsulated in the same in situ hydrogel, by which controlled-combination therapy can be achieved.
[0063] The hydrogel has an aqueous environment inside. For labile biomolecues, the aqueous environment inside the hydrogel versus a hydrophobic environment inside a traditional polymer implant enables the labile biomolecules to maintain correct three-dimensional structure and enhances stability of the labile biomolecules and helps to maintain therapeutic efficacy of the labile biomolecules. Similarly, drug encapsulating particles, after being encapsulated in the hydrogel, will not contact the blood/lymphatic system, reducing the chance of being eliminated. In the eye, this encapsulation also reduces the risk of elicit adverse effects, such as sterile endophalmitis by contacting ocular tissue.
[0064] The hydrogel formation and therapeutic molecule encapsulation occur at mild physiological conditions. In an embodiment, mild physiological conditions refer to a pH from about 5 to about 9, a temperature from about 10 to about 40 degrees Celsius, or a water content of at least about 90%. In another embodiment, mild physiological conditions refer to a pH of about 7.4, a pressure of about 1 atm, a temperature of about 37 degrees Celsius, or a water content of at least about 99%.
[0065] The hydrogel drug delivery system can facilitate controlled drug delivery to the site. The hydrogel drug delivery system is useful for prolonged delivery of therapeutics to the site. Therapeutics can be delivered to the site for days, months or years. Because of the in situ gelatation property of the hydrogel, the release rate of the therapeutic molecule can be controlled, for example, by controlling the crosslinking density. Additionally, the release rate can be further controlled by selecting different polymers for the release of different drugs. For example, when long term release is desirable, a positively charged drug, like Avastin, can be better trapped in a negatively charged polymer, like multi-vinylsulfone hyaluranic acid.
[0066] Referring now to FIG. 6, illustrated is an example non-limiting process flow diagram of a method 600 for forming a hydrogel encapsulating a therapeutic material at a site in the body, according to an embodiment. Method 600 refers to an in situ forming hydrogel formulation for controlled delivery of therapeutics to a site in the body. In an embodiment, the therapeutics are macromolecule and/or small molecular therapeutics and the site the body is the eye.
[0067] At element 602, components are dissolved and mixed in an aqueous solution. The components include polymers with multiple vinylsulfone groups per molecule formed according to methods 100-300, molecules having multiple thiols per molecule, and therapeutic molecules and/or therapeutic molecule-encapsulated particles.
[0068] At element 604, the aqueous solution with the mixed components is injected to a site in the body. According to an embodiment, the site in the body is the eye. After injection the polymers with multiple vinylsulfone groups per molecule formed according to methods 100-300 and the molecules having multiple thiols per molecule are crosslinked and the therapeutic material is encapsulated within the crosslinked network at mild physiological conditions. At element 606, a hydrogel is formed that encapsulates the therapeutic material with a controlled gelatation time. The formation and encapsulation are each in situ processes. The gelatation time
is well controlled so that the hydrogel is completely formed shortly after injection, but not too fast to allow manipulation of the therapeutic material. In an embodiment, the gelatation time sufficient to allow complete encapsulation of the therapeutic material, but shorter than a time of elimination of the free therapeutic material via circulation of the blood or lymph.
EXPERIMENTAL
[0069] The following examples illustrate modification of hyaluranic acid, dextran, polyvinyl alcohol, alginate and polyethylene glycol with vinylsulfone groups. However, it should be noted that the methods 100-600 are not limited to merely these polymers; instead, methods 100-600 are applicable to all hydroxyl containing water soluble polymers. The values of reaction variables, such as, the concentration of the polymers, pH, vinylsulfone to hydroxide ratio, and the like, and/or the protocols of the method, such as, the purification procedure, choice of polymer, choice of thiol containing molecules, reaction time, reaction buffer, and the like can be changed to control the addition of vinylsulfone groups to the polymers in the formation of the modified polymers. The vinylsulfone groups of the modified polymers can participate in a subsequent thiol-Michael "click" reaction with a thiol counterpart.
[0070] The following examples are exemplary or illustrative of the application of the principles described above. It will be noted that experimental data provided does not limit the scope of the embodiments. Rather, such data merely illustrate the preparation of composition embodiments in accordance with the subject innovation as well as for demonstrating the properties described above illustrating the usefulness of the composition for drug delivery.
Synthesis of modified molecule
Synthesis of vinylsulfone-modified hyaluranic acid
[0071] Hyaluranic acid was dissolved in 0.1 M NaOH at 2% w/v (corresponding to approximately 200 μπιοΐ hydroxyl groups per ml). Divinylsulfone was added into a vigorously vortexing hyaluranic acid solution in excess at a molar ratio of 1.25-times the hydroxyl groups of hyaluranic acid. The reaction was carried out for 10 minutes and stopped by adjusting the pH to 5 using 5M HC1. After adjusting the pH, the solution was purified by dialysis and freeze-dried.
[0072] The success of conjugation was confirmed by 1H NMR, as shown in FIG. 7. FIG.
7(A) relates to unmodified hyaluranic acid and FIG. 7(B) relates to hyaluranic acid modified with vinylsulfone. Element 702 is an illustration of the chemical structure of unmodified hyaluranic acid and element 704 is an illustration of the chemical structure of hyaluranic acid modified with vinylsulfone. Element 706 is the 1H NMR spectrum of unmodified hyaluranic acid and element 708 is the 1H NMR spectrum of hyaluranic acid modified with vinylsulfone.
[0073] The NMR signals of free vinylsulfone double bonds are at δ= 6.3 (f ), 6.4 (e') and
6.9 (d') in element 708 of FIG. 7(B). The degree of modification, defined as the number of vinylsulfone groups divided by the number of disaccharide repeating units, was calculated from 1H NMR spectra by comparing the integral signals at δ= 6.9 and at δ= 2 (acetyl group of the disaccharide).
Synthesis of vinylsulfone-modified dextran
[0074] Dextran was dissolved in 0.1 M NaOH by 2% w/v. A 1.5x excessive (molar ratio to hydroxyl groups of the polymer) divinylsulfone was added into a vigorously vortexing polymer solution. The reaction was stopped by adjusting the pH to 5 with 5M HCl. After the pH adjustment, the solution was purified by dialysis and freeze-dried. FIG. 8, elements 802 and 804, confirm the success of conjugation.
Synthesis of vinylsulfone-modified polyvinyl alcohol
[0075] Polyvinyl alcohol was dissolved in 0.1 M NaOH by 2% w/v. A 1.5-times excessive (molar ratio to hydroxyl groups of the polymer) divinylsulfone was added into a vigorously vortexing polymer solution. The reaction was stopped by adjusting the pH to 5 with 5M HCl. After the pH adjustment, the solution was purified by diafiltration and freeze-dried. FIG. 9, elements 902 and 904, confirm the success of conjugation.
Synthesis of vinylsulfone-modified alginate
[0076] Alginate was dissolved in 0.1 M NaOH by 2% w/v. A 1.5-times excessive (molar ratio to hydroxyl groups of the polymer) divinylsulfone was added instantly into the vigorously vortexing polymer solution. The reaction was stopped by adjusting the pH to 5 with 5M HC1. After the pH adjustment, the solution was purified by diafiltration and freeze-dried. FIG. 10, elements 1002 and 1004, confirm the success of conjugation.
Synthesis of vinylsulfone-modifled polyethylene glycol
[0077] Polyethylene glycol was dissolved in 0.1 M NaOH by 6% w/v. A 10-times excessive (molar ratio to hydroxyl groups of the polymer) divinylsulfone was added into the vigorously vortexing polymer solution. The reaction was stopped by adjusting the pH to 5 with 5M HC1. After the pH adjustment, the solution was purified by diafiltration and freeze-dried. FIG. 1 1, elements 1102 and 1104, confirm the success of conjugation.
Controlling the degree of modification
[0078] The degree of modification of a certain hydroxyl containing water soluble polymer can be controlled by at least three factors: reaction pH, reaction time and the molar ratio between divinylsulfone and OH.
[0079] The following examples show how to control the degree of modification of hyaluranic acid and dextran; however, it should be noted that control principle is applicable to other hydroxyl containing water soluble polymers as well.
Controlling the degree of modification of vinylsulfone-modified hyaluranic acid
[0080] A hyaluranic acid solution was dissolved in nanopure water® and adjusted to different pH values (in the range of 9 to 10) by drop- wise addition of 6 M NaOH. Divinylsulfone was added into the vigorously vortexing hyaluranic acid solution, at a molar ratio of 1.25-times in excess of the hydroxyl groups of hyaluranic acid.
[0081] The reaction was carried out for 12 hours and stopped by adjusting the pH to 5 using 5M HC1. For the time-controlled experiment, HA was dissolved in 0.01 M or 0.1 M NaOH
solution at 2% w/v. Divinylsulfone was added into the vigorously vortexing hyaluranic acid solution at a molar ratio of 1.25-times the hydroxyl groups of hyaluranic acid. The reactions were stopped at predetermined time points by adjusting the pH to 5 using 5M HCl.
[0082] To investigate the changing molar ratio of divinylsulfone: OH, hyaluranic acid was dissolved in 0.1 M NaOH and divinylsulfone was added instantly into the vigorously vortexing hyaluranic acid solution at a molar ratio of 1.25, 2.5, or 10 times the hydroxyl groups of hyaluranic acid. The reactions were stopped at pre-determined time points by adjusting the pH to 5 using 5M HCl. After the pH adjustment, the solution was purified by diafiltration and freeze-dried.
[0083] The success of conjugation and the degree of modification was examined by Ή
NMR. A table illustrating the types of modification for hyaluranic acid is shown in FIG. 13. Vinylsulfone-modified hyaluranic acid with degrees of modification lower than 3% and as high as 160% was synthesized.
Controlling the degree of modification of vinylsulfone-modified dextran
[0084] Dextran was dissolved in 0.025 M NaOH solution and 1.2-times divinylsulfone was added to the vigorously stirring dextran solution. The reactions were stopped at
predetermined time points by adjusting the pH to 5 using 5M HCl. After the pH adjustment, the solution was purified by dialysis or diafiltration or other types of methods and freeze-dried. The success of conjugation and the DM was examined by 1H NMR, as illustrated in FIG . 13.
Cytotoxicity of vinylsulfone-modified polymer
[0085] To examine whether a vinylsulfone group conjugated on a polymer is toxic to a cell, a Live/Death assay was used for testing cytotoxicity of vinylsulfone-modified hyaluranic acid.
[0086] NIH 3T3 cells were cultured on a 96 well plate, and vinylsulfone-modified hyaluranic acid of concentration 0.1% to 1% was added to the cell and incubated for 5 hours or 20 hours before the assays were performed. As shown in FIG. 14, no cytotoxic effect were observed (in the assays, live cells appear green and dead cells appear red; no red was observed).
Reaction of vinylsulfone-modified polymers with thiols
[0087] The following examples demonstrated that the vinylsulfone modified polymers can react with thiol at mild aqueous conditions. Since these conditions are compatible with labile biomolecules, cells, animals and humans, the vinylsulfone modified polymers are excellent materials for preparing in situ hydrogel, polymer-drug conjugate, protein encapsulation, surface modification, or the like.
Reaction of vinylsulfone-modified hyaluronic acid with dithiothreitol and the preparation of in situ hydrogel
[0088] Vinylsulfone-modified hyaluranic acid was dissolved in an aqueous buffer solution, for example 0.1M, pH 7.4 phosphate buffer (PB), at various concentrations, at 7% w/v. Dithiolthreitol, which is a small molecules containing two thiols was dissolved in the same buffer solution at O.lmg/μΐ and added to the polymer solution at the molar ratio of 1 :1/SH:VS. The gelatation kinetics 1504 and pictures of the actual gel 1502 are shown in FIG. 15.
Reaction of vinylsulfone-modified dextran with dithiothreitol and the preparation of in situ hydrogel
[0089] Vinylsulfone-modified dextran was dissolved in an aqueous buffer solution, for example 0.1M pH 7.4 phosphate buffer (PB), at various concentrations at 7% w/v. The crosslinker dithiothreitol was dissolved in the same buffer solution at O.lmg/μΐ and added to the polymer solution at the molar ratio of 1 :1/SH:VS. The gelatation kinetics 1506 and pictures of the actual gel 1508 are shown in FIG. 15.
Conjugating reduced glutathione on vinylsulfone-modified hyaluranic acid
[0090] Vinylsulfone-modified hyaluranic acid was dissolved in an aqueous buffer solution, for example, 0.1M pH 7.4 PB, at 1% w/v. Two-time excessive (molar ratio to vinylsulfone group) glutathione was added to polymer solution. The reaction was carried out for
2 hours at room temperature and the produced was thoroughly dialysis and freeze dried. The success of conjugation was examined by 1H NMR, as shown in FIG. 16. Element 1602.
Conjugating reduced glutathione on vinylsulfone-modified dextran
[0091] Vinylsulfone-modified dextran was dissolved an aqueous buffer solution, for example, 0.1M pH 7.4 PB, at 1% w/v. Two-time excessive (molar ratio to vinylsulfone group) glutathione was added to polymer solution. The reaction was carried out for 2 hours at room temperature and the produced was thoroughly dialysis and freeze dried. The success of conjugation was examined by 1H NMR, as shown in FIG. 16, element 1604.
Compatibility of vinylsulfone grafted polymer with a rabbit eve
[0092] To examine if the vinylsulfone group grafted on polymer is toxic to eye, vinylsulfone grafted hyaluranic acid was used as an example. Vinylsulfone grafted hyaluranic acid was dissolved in PBS at 10% w/v and injected to the rabbit eye by intravitreal injection. The retina of the rabbit was examined using binocular indirect microscope (BIO).
[0093] No hemorrhage, retinal detachment, edema, neovascularization or any other damages was observed both at day 7 and after 1 month. FIG. 17 shows a representative binocular indirect microscope image.
Crosslinking vinylsulfone grafted polymers with small molecule crosslinker
[0094] Polymers having two or more vinylsulfone groups per each molecule can be crosslinked by small molecules having two or more thiols. The following are examples of two vinylsulfone grafted polymers, vinylsulfone grafted hyaluranic acid and vinylsulfone grafted dextran crosslinked by a small dithiol molecule dithiothreitol at physiological pH.
[0095] It should be noted that this method is not limited to these two polymers and the particular crosslinking molecules we used, and the detail protocol used, for example the specific buffer, pH, concentration, purification method , and the like, are merely examples.
Reaction of vinylsulfone grafted hyaluranic acid with dithiothreitol and the preparation of in situ hydrogel
[0096] Vinylsulfone grafted hyaluranic acid was dissolved in an aqueous buffer solution, for example 0.1M pH 7.4 phosphate buffer saline (PBS), at various concentrations.
[0097] Dithiolthreitol, which is a small molecules containing two thiols was dissolved in the same buffer solution at O.lmg/μΐ and added to the polymer solution at the molar ratio of
1 : 1/SH:VS.
[0098] A hydrogel is formed shortly after mixing.
Reaction of vinylsulfone grafted dextran with dithiothreitol and the preparation of in situ hydrogel
[0099] Vinylsulfone grafted dextran was dissolved in an aqueous buffer solution, for example PBS, at various concentrations. The crosslinker dithiothreitol was dissolved in the same buffer solution at 0. lmg/μΐ and added to the polymer solution at the molar ratio of 1 : 1/SH:VS. A hydrogel was formed shortly after mixing.
Crosslinking vinylsulfone grafted polymers with thiol containing polymers
[00100] Polymers having two or more vinylsulfone groups per each molecule can be crosslinked by another large molecule, for example polymers, having two or more thiols per molecule. The following are examples of two VS grafted polymers: vinylsulfone grafted hyaluronic acid and vinylsulfone grafted dextran, crosslinked by two thiolated polymer thiolated hyaluronic acid (HA-SH) and thiolated dextran (dextran-VS).
[00101] It should be noted that this method is not limited to these two polymers, and the detailed protocol used, for example the specific buffer, pH, concentration, purification method, and the like, are merely examples.
Synthesis of HA-SH
[00102] Vinylsulfone grated hyaluronic acid was dissolved in a pH 7.4 buffer solution, for example 0.1M pH 7.4 phosphate buffer (PB), by 1% and purged with N2. Equal molar
dithiothreitol (DTT, molar ratio to OH groups of unmodified HA) was added to the reaction by aliquot previously dissolved in buffer solution. The pH is about 7.4 after adding dithiolthreitol.
[00103] The reaction was carried out for 30 minutes, stopped by readjusting pH to 4.5 by 1M HC1, and purified by diafiltration and freeze dried. The success of modification was monitored by the elimination of vinylsulfone double bond from Ή NMR spectrum and Ellman's assay.
Synthesis of dextran-SH
[00104] Vinylsulfone grafted dextran (dextran-VS) was dissolved in a pH 7.4 buffer solution, for example 0.1M pH 7.4 phosphate buffer (PB), by 1% and purged with N2. Equal molar dithiothreitol (DTT, molar ratio to OH groups of unmodified HA) was added to the reaction by aliquot previously dissolved in buffer solution. The pH is about 7.4 after adding DTT. The reaction was carried out for 30 minutes, stopped by readjusting pH to 4.5 by 1M HC1 and purified by diafiltration and freeze dried. The success of modification was monitored by the elimination of vinylsulfone double bond from 1H NMR spectrum and Ellman's assay.
Reaction of vinylsulfone grafted hyaluronic acid with HASH and the preparation of in situ hydrogel
[00105] Vinylsulfone grafted hyaluronic acid and HA-SH were dissolved separately in an aqueous buffer solution, for example PBS, at various concentrations, for example 10% w/v.
Upon mixing, a hydrogel formed shortly.
Reaction of vinylsulfone grafted dextran with dextran-SH and the preparation of in situ hydrogel
[00106] Vinylsulfone grafted dextran and dextran-SH were dissolved separately in an aqueous buffer solution, for example PBS, at various concentrations, for example 10% w/v.
Upon mixing, a hydrogel formed shortly
Reaction of vinylsulfone grafted dextran with HA-SH and the preparation of in situ hydrogel
[00107] Vinylsulfone grafted dextran and HA-SH were dissolved separately in an aqueous buffer solution, for example PBS, at various concentrations, for example 10% w/v. Upon mixing, a hydrogel formed shortly
Encapsulating macromolecules in the in situ hydrogel and the in vitro release
[00108] The following is an example showing the controlled release of macromolecules from the hydrogel in vitro. A hyaluronic acid based hydrogel, either composed of vinylsulfone grafted hyaluronic acid crosslinked by small molecule crosslinker dithiothreitol or polymer crosslinker HA-SH, and three model proteins bovine serum albumin (BSA), near infrared labeled IgG (NIR-IgG) and Avastin, were used as a model polymer and macromolecule.
[00109] It should be noted that, the choice of polymer is highly dependent on the drug used. For example, Avastin is a full length antibody drug widely used for treating various eye diseases, including age-related macular degeneration. Avastint has molecular weight of 150 kDa and is positively charged at a neutral pH.
[00110] Thus, if desirable, a negatively charged polymer hyaluranic acid can be used to prolong the release of the drug.
[00111] When necessary, polymers of different charges can be mixed to give the most suitable release kinetics.
Hydrogel made from vinylsulfone grafted hyaluronic acid crosslinked with dithiothreitol and the release of BSA
[00112] BSA was dissolved in a pH 7.4 buffer solution, at various concentration from 0.1% to 10% w/v. vinylsulfone grafted hyaluranic acid was dissolved in this protein solution. The crosslinker dithiothreitol was dissolved in the same buffer solution at O.lmg/μΐ and added to the vinylsulfone grafted hyaluranic acid/BSA solution at the molar ratio of 1 :1/SH:VS.
[00113] Gel was formed after mixing, and the protein was encapsulated in the gel. PBS was then added as sink for the protein to release. Protein (BSA) release data for more than two months was shown in FIG. 18. Less than 30% of the protein was released.
Hydrogel made from vinylsulfone grafted hyaluronic acid crosslinked with HASH and the release ofNIR-IgG and Avastin
[00114] Vinylsulfone grafted hyaluranic acid and HA-SH was dissolved in PBS at separately. An antibody was added to the polymer right before mixing of the two polymers. After mixing, the polymer and drug mixture was incubated overnight to ensure complete gelatation. PBS was then added as sink for the protein to release.
[00115] Protein release data for more than one month was shown in FIG. 19. More than 95 % of antibody was still retained in this gel, showing excellent controlled release property of this gel.
Encapsulating drug-encapsulated particles in the hydrogel
[00116] The following example shows how to encapsulate drug-encapsulated particles in the in situ hydrogel. The model drug molecule used is triamcinolone, a steroid drug widely used for treating various ocular inflammation.
[00117] It should be noted that this method is not limited to this particular drug, particular particle and particular vinylsulfone modified polymers and crosslinkers, and the detail protocol used, for example the specific buffer, pH, concentration, purification method, and the like, are only examples.
[00118] Model drug triamcinolone can be encapsulated in two component nanoparticles form by FTAEA and F-moc phenylalanine of diameter about 100 nm. The particles are dissolved in a pH 7.4 buffer solution.
[00119] Vinylsulfone grafted hyaluranic acid is dissolved a pH 7.4 buffer solution and mixed with the nanoparticle solution. HA-SH dissolved in the same buffer solution as vinylsulfone grafted hyaluranic acid is added to vinylsulfone grafted hyaluranic acid
/nanoparticle mixture. Gel was formed soon after mixing.
Ocular compatibility of hydrogel
[00120] The following are examples showing the biocompatibility of hydrogel in vivo. A hyaluranic acid based hydrogel was used as an example. However, it should be noted that, the choice of polymer and the detail protocol used, for example the specific buffer, pH,
concentration, purification method, and the like, are merely examples.
[00121] Vinylsulfone grafted hyaluranic acid and HA-SH were dissolved in PBS at separately. After mixing, 50 μΐ of the polymer mixture was injected to the rabbit eye by intravitreal injection. The injected eyes were examined by binocular indirect microscope periodically. No hemorrhage, retinal detachment, edema, neovascularization or any other damages was observed in any ocular examination. Representative binocular indirect microscope images are shown in figure 20.
Injection of protein encapsulated in situ hydrogel into a rabbit eve
[00122] The following are examples showing the injection of hydrogel into the rabbit eye and the controlled release of drug from the hydrogel in vivo. A hyaluranic acid based hydrogel and NIR-IgG, which is structurally similar to a widely used anti-VEGF antibody, Avastin, for treating eye diseases, was used as model polymer and drug molecule. However, it should be noted that, the choice of polymer is highly dependent on the drug used, and the detail protocol used, for example the specific buffer, pH, concentration, purification method, and the like, are merely examples.
Sub-Tenon 's injection of protein encapsulated hyaluranic acid in situ hydrogel
[00123] Vinylsulfone grafted hyaluranic acid and HA-SH were dissolved in PBS at separately. NIR-IgG was added right before mixing of the two polymers. After mixing, 600 μΐ of the polymer/drug mixture was injected to the rabbit eye by sub-Tenon's injection (shown in FIG. 21(A)).
[00124] One week later, the rabbit was enucleated and the gel was removed from the sub- Tenon's space. The presence of NIR-IgG in the sclera was examined by NIR fluorescence
imager. The fluorescence in the sclera of treated eye indicates the release of drug in vivo in FIG. 21(B).
Intravitreal injection of protein encapsulated hyaluronic acid in situ hydrogel
[00125] Vinylsulfone grafted hyaluranic acid and HA-SH were dissolved in PBS separately. An antibody was added to the polymer right before mixing of the two polymers.
[00126] After mixing, 50 μΐ of the polymer/drug mixture was injected to the rabbit eye by intravitreal injection. One week later, the rabbit was killed and enucleated. The eye was bisected and the presence of NIR-IgG inside the eye was examined by NIR fluorescence imager.
[00127] FIG. 22 is a picture of the bisected rabbit eye ball. A transparent hydrogel is clearly seen surrounded by the vitreous.
[00128] FIG. 23 shows the comparison of vitreous from treated eye and control eye. The fluorescence in the vitreous of treated eye indicates the release of drug in vivo.
[00129] What has been described above includes examples of the embodiments of the subject disclosure. It is, of course, not possible to describe every conceivable combination of components or methods for purposes of describing the claimed subject matter, but it is to be appreciated that many further combinations and permutations of the various embodiments are possible. Accordingly, the claimed subject matter is intended to embrace all such alterations, modifications, and variations that fall within the spirit and scope of the appended claims. While specific embodiments and examples are described in this disclosure for illustrative purposes, various modifications are possible that are considered within the scope of such embodiments and examples, as those skilled in the relevant art can recognize.
[00130] In addition, the words "example" or "exemplary" is used herein to mean serving as an example, instance, or illustration. Any aspect or design described herein as "exemplary" is not necessarily to be construed as preferred or advantageous over other aspects or designs. Rather, use of the word exemplary is intended to present concepts in a concrete fashion. As used in this application, the term "or" is intended to mean an inclusive "or" rather than an exclusive "or". That is, unless specified otherwise, or clear from context, "X employs A or B" is intended to mean any of the natural inclusive permutations. That is, if X employs A; X employs B; or X
employs both A and B, then "X employs A or B" is satisfied under any of the foregoing instances. In addition, the articles "a" and "an" as used in this application and the appended claims should generally be construed to mean "one or more" unless specified otherwise or clear from context to be directed to a singular form.
[00131] In addition, while an aspect may have been disclosed with respect to only one of several embodiments, such feature may be combined with one or more other features of the other embodiments as may be desired and advantageous for any given or particular application.
Furthermore, to the extent that the terms "includes," "including," "has," "contains," variants thereof, and other similar words are used in either the detailed description or the claims, these terms are intended to be inclusive in a manner similar to the term "comprising" as an open transition word without precluding any additional or other elements.
[00132] Numerical data, such as temperatures, concentrations, times, ratios, and the like, are presented herein in a range format. The range format is used merely for convenience and brevity. The range format is meant to be interpreted flexibly to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within the range as if each numerical value and sub-range is explicitly recited. When reported herein, any numerical values are meant to implicitly include the term "about." Values resulting from experimental error that can occur when taking
measurements are meant to be included in the numerical values.
Claims
1. A drug delivery system, comprising:
a multi-vinylsulfone containing molecule;
a multi-thiol containing molecule; and
a therapeutic molecule,
wherein:
the drug delivery system dissolves in water to form an aqueous solution, and
the aqueous solution undergoes gelatation upon administration to a site in a body.
2. The drug delivery system of claim 1, wherein the aqueous solution undergoes the gelatation when the multi-vinylsulfone containing molecule forms a covalent bond with the multi-thiol containing molecule.
3. The drug delivery system of claim 2, wherein the therapeutic molecule is encapsulated within a network formed by the multi-vinylsulfone containing molecule and the multi-thiol containing molecule.
4. The drug delivery system of claim 1, wherein the therapeutic agent is a
biomacromolecule or a particle encapsulating a drug molecule.
5. The drug delivery system of claim 1, wherein the drug delivery system is administered by an injection to a surface of the body or to an interior of the body.
6. The drug delivery system of claim 1, wherein the drug delivery system is administered to the body by an intravitreal injection, a peribulbar injection, or a subtenon injection.
7. The drug delivery system of claim 1, wherein the multi-vinylsulfone containing molecule is a polymer.
8. The drug delivery system of claim 7, wherein the polymer is derived from a hydroxyl containing polymer.
9. The drug delivery system of claim 1 , wherein
the aqueous solution undergoes the gelatation and forms a hydrogel, and
the therapeutic molecule is released from the hydrogel by diffusion of the therapeutic agent from the hydrogel or by degradation of the hydrogel
10. A method, comprising:
dissolving a water soluble polymer containing a hydroxyl group in an aqueous solution to form a polymer solution;
adding a molecule containing two vinylsulfone groups to the polymer solution; and forming a modified polymer by controlling a number of the vinylsulfone groups that are grafted on the polymer, wherein the vinylsulfone groups grafted on the polymer are chemically reactive.
1 1. The method of claim 10, wherein the dissolving further comprises dissolving the water soluble polymer in the aqueous solution comprising a salt or an organic solvent.
12. The method of claim 10, wherein the dissolving further comprises dissolving the water soluble polymer in an alkaline aqueous solution.
13. The method of claim 10, wherein the controlling further comprises varying a reaction time, an amount of molecules containing two vinylsulfone groups, or a basicity of the aqueous solution.
14. The method of claim 10, further comprising covalently bonding the modified polymer and a molecule containing a nucleophile.
15. The method of claim 14, wherein the nucleophile is a thiol or an amine.
16. The method of claim 14, wherein the covalenly bonding further comprises covalently boding the modified polymer and the molecule containing the nucleophile under aqueous conditions with a pH from about 5 to about 9, a temperature from about 10 to about 40 degrees Celsius, or a water content of at least about 90%.
17. The method of claim 14, wherein the covalently bonding further comprises covalently boding the modified polymer and the molecule containing the nucleophile under physiological aqueous conditions with a pH of about 7.4, a temperature of about 37 degrees Celsius, and a water content of at least about 99%.
18. A hydrogel, comprising:
a multi-vinylsulfone containing molecule, and
a multi-thiol containing molecule, wherein
the hydrogel is formed at a site of a biological tissue from an aqueous solution comprising the multi-vinylsulfone containing molecule and the multi-thiol containing molecule upon delivery to the site by a covalent bond between the multi-vinylsulfone containing molecule and the multi-thiol containing molecule.
19. The hydrogel of claim 18, wherein the multi-vinylsulfone containing molecule is a polymer containing at least one vinylsulfone group.
20. The hydrogel of claim 18, wherein the multi-thiol containing molecule is a polymer containing two or more thiol groups.
21. The hydrogel of claim 18, wherein the multi-vinylsulfone containing molecule or the multi-thiol containing molecule is a polysaccharide derivative.
22. The hydrogel of claim 18, further comprising free vinylsulfone groups or thiol groups for interacting with therapeutics or the biological tissue.
23. The hydrogel of claim 22, wherein the aqueous solution comprises a salt, an organic solvent, a therapeutic agent or a molecule that modulates an extent of the free vinylsulfone groups and thiol groups.
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US14/126,725 US9592251B2 (en) | 2011-06-16 | 2012-06-15 | Multi-vinylsulfone containing molecule |
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CN105209075A (en) * | 2013-04-18 | 2015-12-30 | 香港科技大学 | Biocompatible in situ hydrogel |
US9844597B2 (en) | 2013-04-18 | 2017-12-19 | The Hong Kong University Of Science And Technology | Biocompatible in situ hydrogel |
CN105209075B (en) * | 2013-04-18 | 2019-12-13 | 香港科技大学 | Biocompatible in situ hydrogels |
WO2014169708A1 (en) * | 2013-04-18 | 2014-10-23 | The Hong Kong University Of Science And Technology | Biocompatible in situ hydrogel |
US20150250815A1 (en) * | 2014-03-10 | 2015-09-10 | Kai-shun Christopher LEUNG | Induction of chronic elevation of intraocular pressure with intracameral cross-linking hydrogel |
US9895394B2 (en) * | 2014-03-10 | 2018-02-20 | Kai-shun Christopher LEUNG | Induction of chronic elevation of intraocular pressure with vinysulfonated hyaluronic acid (HA-VS) and thiolated hyaluronic acid (HA-SH)hydrogel |
US11642415B2 (en) | 2017-03-22 | 2023-05-09 | Ascendis Pharma A/S | Hydrogel cross-linked hyaluronic acid prodrug compositions and methods |
US11440976B2 (en) | 2017-09-01 | 2022-09-13 | Pmidg, Llc | Functionalized and crosslinked polymers |
WO2019046834A1 (en) * | 2017-09-01 | 2019-03-07 | Pmidg, Llc | Functionalized and crosslinked polymers |
JP2020532643A (en) * | 2017-09-01 | 2020-11-12 | ピーエムアイディージー・エルエルシーPmidg,Llc | Functionalized and crosslinked polymers |
WO2021080345A1 (en) * | 2019-10-24 | 2021-04-29 | 서울대학교병원 | Injectable intraocular microgel as drug delivery system, and hydrogel comprising same |
KR102435274B1 (en) * | 2019-10-24 | 2022-08-24 | 서울대학교병원 | Eye-injecting microgel as drug delivery system and eye-injecting hydrogel having the same |
KR20210049218A (en) * | 2019-10-24 | 2021-05-06 | 서울대학교병원 | Eye-injecting microgel as drug delivery system and eye-injecting hydrogel having the same |
EP4049653A4 (en) * | 2019-10-24 | 2023-11-01 | Seoul National University Hospital | Injectable intraocular microgel as drug delivery system, and hydrogel comprising same |
WO2021143736A1 (en) * | 2020-01-16 | 2021-07-22 | The Hong Kong University Of Science And Technology | Compositions and methods for controlled release of target agent |
EP4090317A4 (en) * | 2020-01-16 | 2024-02-21 | The Hong Kong University of Science and Technology | Compositions and methods for controlled release of target agent |
WO2022120097A1 (en) * | 2020-12-03 | 2022-06-09 | Pmidg, Llc | Functionalized and crosslinked polymers |
Also Published As
Publication number | Publication date |
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US20140212373A1 (en) | 2014-07-31 |
CN103687622A (en) | 2014-03-26 |
EP2720722A4 (en) | 2014-12-03 |
EP2720722A1 (en) | 2014-04-23 |
US9592251B2 (en) | 2017-03-14 |
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