WO2012017405A1 - Microparticle formulation for pulmonary drug delivery of anti-infective molecule for treatment of infectious diseases - Google Patents
Microparticle formulation for pulmonary drug delivery of anti-infective molecule for treatment of infectious diseases Download PDFInfo
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- WO2012017405A1 WO2012017405A1 PCT/IB2011/053470 IB2011053470W WO2012017405A1 WO 2012017405 A1 WO2012017405 A1 WO 2012017405A1 IB 2011053470 W IB2011053470 W IB 2011053470W WO 2012017405 A1 WO2012017405 A1 WO 2012017405A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/12—Cyclic peptides, e.g. bacitracins; Polymyxins; Gramicidins S, C; Tyrocidins A, B or C
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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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4748—Quinolines; Isoquinolines forming part of bridged ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/007—Pulmonary tract; Aromatherapy
- A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
- A61K9/0078—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy for inhalation via a nebulizer such as a jet nebulizer, ultrasonic nebulizer, e.g. in the form of aqueous drug solutions or dispersions
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/127—Liposomes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- A61P31/06—Antibacterial agents for tuberculosis
Definitions
- the present invention also relates to a method of treatment of pulmonary tuberculosis, multi drug resistant tuberculosis (MDRTB), methicillin resistant Staphylococcus aureus (MRSA) pneumonias and methicillin sensitive Staphylococcus aureus (MSSA) pneumonias by administering therapeutically effective amount of the formulation to a mammal in need thereof.
- MDRTB multi drug resistant tuberculosis
- MRSA methicillin resistant Staphylococcus aureus
- MSSA methicillin sensitive Staphylococcus aureus
- the current chemotherapeutic regimen for treating pulmonary tuberculosis consists of coadministration of front-line antitubercular drugs (isoniazid, rifampicin, ethambutol, and/or pyrizinamide) for a period of four months followed by two months of treatment with isoniazid, rifampicin, and/or ethambutol, but depending upon the type of tuberculosis, the treatment can be further extended upto a period ranging from 9 months to 2 years.
- front-line antitubercular drugs isoniazid, rifampicin, ethambutol, and/or pyrizinamide
- Linezolid which is accepted for therapy in MRSA pneumonia, exhibits good oral bioavailability (administered as 600 mg oral twice daily) but is associated with gastrointestinal adverse effects, thrombocytopenia, and reversible anemia (Clinical Infect. Dis., 2003, 37, 1609-1616). On rare occasions, administration of linezolid is also associated with optic and peripheral neuropathy (J Antimivrob. Chemother., 2004, 53, 1 1 14-1 1 15).
- Beta lactam agents are very effective against MSSA pneumonia as first line of therapy.
- vancomycin is considered as next line of therapy, it is not as effective as the beta lactam agents in infections caused by MSSA.
- vancomycin is excreted in the urine by glomerular filtration and is not metabolized. Lung tissue penetration of vancomycin is also relatively poor (US Respiratory Disease, 2006, 62-64).
- the therapy for MRSA/MSSA pneumonia has several drawbacks such as poor pulmonary bioavailability of drugs, drug dosage induced toxicity, etc.
- the present invention relates to a biodegradable, inhalable microparticle formulation comprising compound of formula I (as described herein) obtained by fermentation of a microorganism of the Streptomyces species (PM0626271 /MTCC5447), and a biodegradable lipid for drug delivery wherein the ratio of drug (compound of formula I) to lipid is from 1 :15 to 1 :25.
- the present invention further relates to the use of the microparticle formulation comprising compound of formula I and a biodegradable lipid for drug delivery wherein the ratio of drug (compound of formula I) to lipid is 1 :15 to 1 :25 for the treatment of pulmonary tuberculosis, MDRTB, MRSA pneumonias and MSSA pneumonias.
- Entrapment efficiency is the fraction of drug associated and physically entrapped in the microparticle formulation relative to the initial total amount of drug in the solution.
- Osmolality is a measure of solute concentration, defined as the number of osmoles (mOsm) of solute per kilogram of solvent (mosmol/kg or mOsm/kg).
- phase transition is the transformation of a thermodynamic system from one phase or state of matter to another.
- a phase of a thermodynamic system and the states of matter have essentially uniform physical properties.
- certain properties of the medium change, often discontinuously, as a result of some external condition, such as temperature, pressure, and others.
- the measurement of the external conditions at which the transformation occurs, is termed as the phase transition point.
- Aerosolization Aerosolization is the production of an aerosol - a fine mist or spray containing minute particles.
- Nebulization involves the process of transforming liquid medications into faster-acting inhaled mists. Nebulization is used to treat respiratory conditions, such as asthma or cystic fibrosis. Nebulizers effectively deliver medicine directly into an individual's respiratory tract so that it can reach the lungs quickly.
- a non-limiting example of nebulizer is a machine equipped with a compressor and a mouthpiece or face mask.
- the suspensions contain innumerable number of particles of varying sizes in motion.
- the particle-sizing machine analyzes these particles, it forms a particle distribution curve, which covers the entire particle size range starting from the smallest particle, which could be 1 nm to the largest, which could be 100 microns.
- a cumulative frequency is calculated for the particles.
- D 0 refers to that particular particle diameter where 10 % of the particles in the suspension have a smaller diameter or equal diameter as that of the particular particle diameter.
- D 90 is the cut off diameter for 90 % of the particle population in the formulation and refers to that particular particle diameter where 90 % of the particles in the suspension have a smaller diameter or equal diameter as that of the particular particle diameter.
- Entrapped drug retention on nebulization During nebulization process, due to the force induced by the nebulizer some liposomes rupture and the drug leeches out of the formulation and gets retained in the nebulization cup itself.
- the drug which does not leech out of the formulation during the nebulization process is the actual amount of drug retained in the formulation during nebulization and is designated as "entrapped drug retention".
- the drug which is lost to/leeched out during the nebulization process is recovered from the nebulization cup.
- the nebulization cup is washed with a suitable solvent (in this case methanol) and drug retained in the cup is quantified by HPLC or LC-MS.
- Liquid Crystalline Phase It is a distinct phase of matter observed between the crystalline (solid) and isotropic (liquid) states.
- Intratracheal Instillation It is a method of drug administration wherein the drug is administered through an endotracheal tube or by percutaneous injection into the trachea for the delivery of drugs into the lungs.
- Ventilatory support In medicine, mechanical ventilation is a method to mechanically assist or replace spontaneous breathing. This is achieved by attaching an endotracheal tube of the disease afflicted patient to the ventilator which is designed for the aforesaid purpose. Ventilators work by altering the patient's airway pressure through an endotracheal or tracheostomy tube. Patients with fulminant pneumonia including MRSA pneumonia are subjected to tracheostomy so that their tissue oxygenation is maintained.
- Therapeutically effective amount refers to the amount of drug enough to treat and eliminate the infectious organism of interest in the in vivo conditions.
- the therapeutic amount of compound of formula I present in the microparticle formulation is in the range of 1 % to 5 % (w/w).
- the compound of formula I is structurally represented by the following formula:
- the microorganism which may be used for the production of the compound of formula I is a strain of Streptomyces species (PM0626271/ MTCC 5447), herein after referred to as culture no. PM0626271 , isolated from a soil sample collected from Schirmacher Oasis in Antarctic region.
- Culture no. PM0626271 has been deposited with Microbial Type Culture Collection (MTCC), Institute of Microbial Technology, Sector 39-A, Chandigarh -160 036, India, a World Intellectual Property Organization (WIPO) recognized International Depository Authority (IDA) and has accession number MTCC 5447.
- MTCC Microbial Type Culture Collection
- IDA World Intellectual Property Organization
- the compound can be produced from culture no. PM0626271 , its mutants and variants, comprising the steps of: growing the culture no. PM0626271 under submerged aerobic conditions in a nutrient medium containing one or more sources of carbon and one or more sources of nitrogen and optionally nutrient inorganic salts and/or trace elements; isolating the compound of formula I, from the culture broth; and purifying the compound of formula I, using purification procedures generally used in the art.
- mutants of the microoganism such as those produced by the use of chemical or physical mutagens including X-rays, U.V. rays etc. and organisms whose genetic makeup has been modified by molecular biology techniques, may also be cultivated to produce the compound.
- the medium and/or nutrient medium used for isolation and cultivation of culture no. PM0626271 which produces the compound of formula I, preferably contains sources of carbon, nitrogen and nutrient inorganic salts.
- the carbon sources are, for example, one or more of starch, glucose, sucrose, dextrin, fructose, molasses, glycerol, lactose, or galactose.
- Preferred carbon sources are soluble starch and glucose.
- the sources of nitrogen are, for example, one or more of soybean meal, peanut meal, yeast extract, beef extract, peptone, malt extract, corn steep liquor, gelatin, or casamino acids. Preferred nitrogen sources are peptone and yeast extract.
- the nutrient inorganic salts are, for example, one or more of sodium chloride, potassium chloride, calcium chloride, magnesium chloride, ferric chloride, strontium chloride, cobalt chloride, potassium bromide, sodium fluoride, sodium hydrogen phosphate, potassium hydrogen phosphate, dipotassium hydrogen phosphate, magnesium phosphate, calcium carbonate, sodium bicarbonate, sodium silicate, ammonium nitrate, potassium nitrate, ferrous sulphate, sodium sulphate, ammonium sulphate, magnesium sulphate, ferric citrate, boric acid or trace salt solution such as copper sulphate, manganese chloride or zinc sulphate.
- Calcium carbonate, sodium chloride, and magnesium chloride are the preferred nutrient inorganic salts.
- culture no. PM0626271 may be carried out at a temperature ranging from 22 °C to 36 °C and a pH of about 7.5 to 8.0. Typically, culture no. PM0626271 is maintained at 25 °C to 27 °C and a pH of about 7.4 to 7.8. The well- grown cultures may be preserved in the refrigerator at 4°C to 8°C.
- Seed culture cultivation of culture no. PM0626271 may be carried out at a temperature ranging from 25 °C to 36 °C and a pH of about 7.5 to 8.0 for 66 hours to 75 hours at 200 rpm (revolutions per minute) to 280 rpm.
- culture no. PM0626271 seed is cultivated at 29 °C to 31 °C and a pH of about 7.4 to 7.8, for 72 hours at 230 rpm to 250 rpm.
- the production of the compound of formula I may be carried out by cultivating culture no PM0626271 by fermentation at a temperature ranging from 26 °C to 36 °C and a pH of about 6.5 to 8.5, for 24 hours to 96 hours at 60 rpm to 140 rpm and 100 Ipm (liter per minute) to 200 Ipm aeration.
- culture no. PM0626271 is cultivated at 30 °C to 32 °C and pH 7.4 to 7.8 for 40 hours to 96 hours at 90 rpm and 1 10 Ipm aeration.
- the compound of formula I and isomers thereof can be converted into their pharmaceutically acceptable salts and derivatives, like esters and ethers, which are all contemplated by the present invention.
- 90 % of the microparticles of the formulation are of size less than 10 microns.
- the formulation is an aqueous liposomal dispersion.
- the pH of the formulation is from 6 to 7.
- the osmolality of the formulation is from 300 mOsmol/kg to 400 mOsmol/kg.
- the phase transition temperature of the formulation is from 41 Q C to 43 Q C.
- the formulation can be aerosolized to a mass median aerodynamic diameter of 1 ⁇ to 10 ⁇ by using a nebulizer.
- nebulizers which can be used include but are not limited to Jet nebulizers, Ultrasonic wave nebulizers and Vibrating Mesh nebulizers.
- the present invention also relates to the process for preparation of the microparticle formulation.
- the process for preparation of the formulation involves use of "Solvent evaporation method" which includes the following steps:
- step (b) adding 20 ml_ to 45 ml_ of methanol to the solution of step (a) and mixing well to obtain homogeneous solution;
- step (e) making up the volume obtained in step (d) to 30 ml_ with SLF and centrifuging at 15000 G TO 35000 G, at 4 Q C for ten minutes to obtain a pellet;
- step (f) resuspending the pellet obtained in step (e) in SLF to obtain a suspension of concentration 0.5 img/mL to 10 img/mL;
- the compound of formula I and DPPC are dissolved in a 1 :20 ratio.
- step (a) of the process for preparation of the microparticle formulation the compound of formula I and DPPC are dissolved in 5 to 10 mL of chloroform to obtain a solution.
- step (b) of the process for preparation of the microparticle formulation 30 to 40 ml_ of methanol is added.
- step (c) of the process for preparation of the microparticle formulation 25 to 35 ml_ of SLF is added.
- centrifugation is performed at 20,000 to 30,000 G.
- the pellet in the step (f) of the process for preparation of the microparticle formulation, is resuspended in SLF to obtain a suspension of concentration 1 to 5 img/mL.
- the suspension obtained in step (f) is filtered through 2 ⁇ to 5 ⁇ polycarbonate filter.
- the process for the preparation of the formulation is a "Solvent free lipid self assembly method" which includes the following steps:
- step (ii) subjecting the mixture of step (i) to 100 rpm to 200 rpm rotation at 42 Q C to 45 Q C for one hour to obtain a suspension;
- step (v) filtering the suspension obtained in step (iv) through 0.5 ⁇ - 5 ⁇ polycarbonate filter to obtain uniform particle size of the microparticles formed.
- step (i) of the process for preparation of the microparticle formulation 30 mL to 40 mL of SLF is added to a mixture of compound of formula I and DPPC.
- the compound of formula I and DPPC are dissolved in 1 :20 ratio.
- the suspension obtained in step (iii) is centrifuged at 20,000 G to 35,000 G at 4 Q C for ten minutes to obtain a pellet.
- the pellet obtained in step (iii) is resuspended in SLF to obtain a suspension of concentration 1 mg/mL to 5 img/mL
- the suspension obtained in step (iv) is filtered through 2 ⁇ to 5 ⁇ polycarbonate filter.
- the present invention further relates to the use of the formulation in a method of treatment of pulmonary tuberculosis, MDRTB, MRSA pneumonias and MSSA pneumonias by administering therapeutically effective amount of the formulation to a mammal in need thereof.
- the present invention further relates to the use of the microparticle formulation comprising compound of formula I and a biodegradable lipid for drug delivery wherein the ratio of drug to lipid (compound of formula I) is 1 :15 to 1 :25 for the manufacture of a medicament for the treatment of pulmonary tuberculosis, MDRTB, MRSA pneumonias and MSSA pneumonias.
- the present invention also relates to a method of delivering the microparticle formulation to a mammal in need thereof, wherein the formulation is administered by inhalation or intratracheal instillation for pulmonary delivery.
- the method of inhalation is nebulization in which the compound of formula I is entrapped in the microparticles.
- the dosage of compound of formula I for inhalation ranges between 0.05 and 10 mg/kg body weight/day.
- the method of delivering the microparticle formulation is intratracheal instillation in a patient on ventilatory support system.
- administration by nebulization helps reduce the amount of compound of formula I required for the treatment of pulmonary tuberculosis, MDRTB, MRSA pneumonias and MSSA pneumonias.
- API Active Pharmaceutical Ingredient
- Modified artificial sea water agar Peptone 1 .5 g, yeast extract 0.5 g, ferric chloride 0.007 g, 1 .0 L water (750 ml_ artificial sea water + 250 ml_ demineralised water), agar powder 15.0 g, final pH (at 25 °C) 7.4 to 7.8.
- Composition of the artificial seawater Sodium chloride 24.6 g, potassium chloride 0.67 g, calcium chloride.2H 2 O 1 .36 g, magnesium sulphate.7H 2 O 6.29 g, magnesium chloride.6H 2 O 4.66 g, sodium bicarbonate 0.18 g, demineralised water 1 .0 L, final pH (at 25 °C) 7.8 to 8.2.
- the plate was incubated at room temperature (25 ⁇ 2°C) till colonies were observed. After incubation for one and a half month, the colony which appeared on this medium was streaked on petri plates containing actinomycete isolation agar [Hi Media] prepared in 75 % artificial sea water [Accumix Tm ] (AS-AIA).
- the isolate was purified and was provided culture ID number PM0626271 .
- the culture no. PM0626271 was thus isolated from amongst the growing microorganisms as single isolate.
- composition of the purification medium (Actinomycete Isolation Agar, agarified by 1 .5 % agar agar):
- Glycerol 5.0 mL, sodium caseinate 2.0 g, L-asparagine 0.1 g, sodium propionate 4.0 g, dipotassium phosphate 0.5 g, magnesium sulphate 0.1 g, ferrous sulphate 0.001 g, 1 .0 L water (750 mL Artificial Sea Water + 250 mL demineralised water), agar powder 15.0 g, final pH (at 25 °C) 7.4 to 7.8.
- Composition of the artificial seawater Sodium chloride 24.6 g, potassium chloride 0.67 g, calcium chloride.2H 2 O, 1 .36 g, magnesium sulphate.7H 2 O 6.29 g, magnesium chloride.6H 2 O 4.66 g, sodium bicarbonate 0.18 g, demineralized water 1 .0 L, final pH (at 25 °C) 7.8 to 8.2.
- the culture no. PM0626271 was streaked on Actinomycete Isolation Agar (containing 75 % artificial sea water salts) petriplate. The petriplate was incubated for 10 days at 25 °C. One of the isolated colonies from the petriplate was transferred to fresh slants of Actinomycete Isolation Agar prepared in 75 % artificial seawater. The slants were incubated for 10 days at 25 °C.
- Composition of the artificial sea water Sodium chloride 24.6 g, potassium chloride 0.67 g, calcium chloride.2H 2 O 1 .36 g, magnesium sulphate.7H 2 O 6.29 g, magnesium chloride.6H 2 O 4.66 g, sodium bicarbonate 0.18 g, demineralized water 1 .0 L, final pH (at 25 °C) 7.8 to 8.2.
- the production flasks were incubated on shaker at 29 °C and 220 rpm for 96 hours.
- the production flasks were harvested and the whole broth from each media flask was extracted with equal volume of methanol under shaking condition for one hour at 29 °C and centrifuged at 3500 rpm for half an hour. The supernatant was used for antibacterial agar well diffusion assay for monitoring of the activity.
- Artificial Sea Water artificial sea water salt 28.32 g (75 %), soluble starch 20 g, glucose 15 g, yeast extract 2 g, peptone 3 g, calcium carbonate 2 g, ammonium sulphate 0.05 g, corn steep liquor 2 g, sodium chloride 2 g, magnesium phosphate 5 g, cobalt chloride (cobalt chloride 1 g demineralized water 1 .0 L) 1 mL/L, trace salt solution (copper sulphate 7 g, ferrous sulphate 1 g, manganese chloride 8 g, zinc sulphate 2 g, demineralized water 1 .0 L) 1 mL/L, demineralized water 1 .0 L, pH 6.5 to 7.5 (before sterilization).
- Fermentation parameters The fermentation was carried out at temperature 29°C to 30°C, agitation 100 rpm, aeration 60 Ipm and harvested at 70 hours to 74 hours.
- the production of the compound of formula I in the fermentation broth was detected qualitatively by testing the bioactivity against S. aureus E710 (MRSA strain) and/or Enterococcus faecium R2 (VRE) using the agar well diffusion method.
- the harvest pH of the culture broth was 7.5 to 8.0. After the harvest, whole broth was subjected to solvent extraction.
- MRSA strain MRSA strain
- VRE Enterococcus faecium R2
- SLF was prepared by method based on Respiratory Physiology & Neurobiology, 2008, 162, 73-79.
- Compound of formula I exhibits poor solubility in SLF at 45 Q C and 60 Q C. The solubility is also not time dependent. Compound of formula I is a water insoluble compound, thus solubility was measured in the buffer SLF.
- the assay was carried out based on the reference US 4877561 .
- the compound of formula I and DPPC in ratios of 1 :1 , 1 :10 and 1 :20 w/w, were dissolved in 5 mL chloroform in a glass beaker. 30 mL of methanol was added and the mixture was transferred to a 250 mL round bottomed flask. 30 mL of SLF was poured into the mixture slowly. The solvents were evaporated by using a rotary evaporator (Buchi GMBH, Switzerland). The water bath was set at 45 Q C and rotation was set at 100 rpm. The vacuum controller was set to a pressure of 400 mBar. Evaporated solvents were collected in a glass solvent collector.
- the remaining solution in the RB flask turned milky indicating formation of liposomes.
- Volume of the suspension from the RB flask was made up to 30 mL with SLF, centrifuged at 25,000G at 4 Q C for 10 minutes. The pellet obtained was resuspended in SLF, vortexed and filtered through 1 .2 ⁇ polycarbonate filter eleven times to ensure uniform particle size and stored at 4 Q C.
- the microparticle formulation was analyzed by optical microscopy and electron microscopy.
- the aim is to develop a solvent free manufacturing process for the formulation.
- Formulation of microparticles containing compound of formula I and DPPC is optimally formed using drug: lipid ratio of 1 :20 w/w.
- Compound of formula I was dissolved in 20 % DMSO to obtain 200 ⁇ g/mL concentration and was used as reference standard.
- 100 ⁇ L ⁇ of formulation of Example 9 Method A and 100 ⁇ L ⁇ of formulation of Example 9 Method B separately were pipetted into 2 mL centrifuge tubes and 900 ⁇ L ⁇ of 20 % DMSO was added to each tube. The tubes were vortexed which led to the rupture of microparticle matrix and release of entire content of compound of formula I entrapped within the matrix.
- the samples injected independently on the HPLC were as follows: reference standard, formulation of Example 9 Method A (after rupture of the microparticle matrix) and formulation of Example 9 Method B (after rupture of the microparticle matrix). Mean of the peak areas was considered for calculation.
- W amount of drug (compound of formula I) associated/ entrapped within the microparticle
- compound of formula I was recovered from the glassware, filters, all the other labware which was used in the formulation preparation process (Example 9 Method A and Example 9 Method B) and its content was estimated.
- the polycarbonate filters (Example 9 Method A and Example 9 Method B) were washed with 5 mL of 20 % DMSO in methanol. This sample was injected in HPLC as 'membrane residue'.
- the RB flask used to prepare the formulation was washed with 10 mL of 20 % DMSO in methanol. This sample was injected in HPLC as 'flask residue'.
- the reference standard was injected six times on the HPLC and peak areas were noted. The relative standard deviation of six injections of the standard was below 2.0 %. The samples were injected in duplicate on the HPLC and mean of the peak areas were considered for calculation.
- TSI Unit was used for this study and was assembled as per the instruction manual.
- TSI is an in vitro glass model of the human pulmonary tract and is used to quantify in vitro the pulmonary drug deposition potential.
- the vacuum pump of the TSI was switched on and the flow meter was used to accurately check the flow of the system.
- the flow valve on the vacuum pump was adjusted to ensure exact flow specification (28.3 L/min).
- the whole unit was disassembled. 7 mL of methanol was added to the upper impinger and 20 mL methanol was added to the lower impinger.
- the TSI unit was assembled again as per the instruction manual.
- Example 9 Method A 5mL of the formulation of Example 9 Method A was added to the medication cup of the nebulizer. Mouthpiece of the nebulizer was attached to the mouth of the TSI. It was ensured that all parts were fit to avoid any vacuum loss.
- Composition A B :: 50 : 50 (Isocratic)
- the reference standard was injected six times on the HPLC and peak areas were noted. The relative standard deviation of six injections of the standard was below 2.0 %. The samples were injected in duplicate on the HPLC and mean of the peak areas were considered for calculation.
- the formulation when nebulized at a concentration of 1 mg/mL and 2.5 mg/mL deposits about 16 % and 10 % of the initial amount of compound of formula I introduced into the nebulizer cup.
- the minimum inhibitory concentration of compound of formula I is in the range of 0.125 g/mL to 5 g/mL (PCT application publication WO201 1027290).
- the amount of compound of formula I deposited is sufficient and above the minimum inhibitory concentration in the in vitro model.
- 1 mg/mL and 2.5 mg/mL compound of formula I formulation concentrations could be the concentrations which need to be evaluated in the in vivo studies.
- Example 9 Method A is capable of depositing significant amount of compound of formula I in the TSI in vitro lung model while the unformulated compound of formula I is not deposited in the TSI on nebulization.
- the formulation of Example 9 Method A can be used for inhalation-based delivery of compound of formula I.
- the assay was carried out based on the reference; Nathan P et al, 1978, Laboratory Methods for Selection of Topical antimicrobial Agents to treat infected Burn Wounds, Burns 4: 177-187.
- VRE Enterococcus faecium R-2
- Samples tested in the assay are: (i) Sample 1 : Unfiltered suspension of the formulation of Example 9 Method B.
- Sample 3 Sample prepared by methanol disruption method: Sample 2 was mixed with equal volumes of methanol and incubated for one hour. Dilutions of this solution were prepared in methanol and used for evaluating the efficacy of the released compound of formula I.
- concentrations of samples 1 , 2, 3 and 4 evaluated in the assay were: 100, 50, 25, 12.5, 6.25, 3.125, 1 .56, 0.78, 0.39 and 0.195 ⁇ g/mL.
- Sample 3 showed clear zones from 100 ⁇ g/mL to 0.78 ⁇ g/mL while sample 4 showed clear zones from 100 ⁇ /mL to 0.39 ⁇ g/mL.
- sample 2 The activity (with respect to zone size) of sample 2 is better than sample 1 as sample 2 showed clear zone of inhibition at 12 ⁇ g/ml while sample 1 showed clear zones at 25 ⁇ g/ml .
- the zone size of compound of formula I is less than the unformulated compound of formula I (sample 4). This may be due to the slow release of compound of formula I from the lipid formulation.
- Example 18 The activity of compound of formula I released from the formulation of Example 9 Method B (sample 3) is comparable to the unformulated compound of formula I (sample 4) and hence can be carried forward for in vivo testing and evaluation.
- Example 18 The activity of compound of formula I released from the formulation of Example 9 Method B (sample 3) is comparable to the unformulated compound of formula I (sample 4) and hence can be carried forward for in vivo testing and evaluation.
- Example 18 The activity of compound of formula I released from the formulation of Example 9 Method B (sample 3) is comparable to the unformulated compound of formula I (sample 4) and hence can be carried forward for in vivo testing and evaluation.
- Example 18 The activity of compound of formula I released from the formulation of Example 9 Method B (sample 3) is comparable to the unformulated compound of formula I (sample 4) and hence can be carried forward for in vivo testing and evaluation.
- Example 18 The activity of compound of formula I released from the formulation of Example 9 Method B (sample 3) is comparable
- the assay was carried out based on the reference Journal of Biomedical Materials Research, 2009, 89A, 281 -292.
- Time points 24 hours and 48 hours.
- the toxicological evaluation was done using The CellTiter 96 Aqueous One Solution Assay by Promega (Cat.no: G3582).
- the assay is a standard colorimetric method for determining the number of viable cells in proliferation or cytotoxicity assays.
- the MTS used in the assay is bioreduced by cells into a colored formazan product that is soluble in tissue culture medium.
- the quantity of formazan product as measured by the amount of 490 nm absorbance is directly proportional to the number of living cells in culture.
- the cell lines were plated in triplet with 96-well plate and allowed to adhere and proliferate over a period of 24 hours. 24 hours after cell adhesion, the compounds were added. 48 hours post cell plating, the assay was terminated by replacing the medium with 100 ⁇ _ fresh medium, and addition of 20 ⁇ _ of CellTiter 96 Aqueous One Solution (Promega, Cat.no: G3582). A set up in triplet of "no-cell" control containing 100 ⁇ _ of culture medium and 20 ⁇ _ of "One Solution” was also maintained as control in the assay. The plate was incubated for 30 minutes to 4 hours for the color to develop.
- the ELISA 96-well plate was then subjected to absorbance recordings at 490 nm (450-540 nm) with a 96-well plate reader.
- the average 490 nm absorbance from the "no-cell” control was subtracted from all other absorbance values and the corrected absorbance was utilized for further calculations. (Background absorbance from "no-cell” control is typically 0.2 to 0.3 absorbance units after 4 hours of incubation).
- Sample 3 has the potential to result or express in vivo adverse effects and toxicity. However sample 1 that includes the use of DPPC, the toxic potential of compound of formula I is masked and biological efficacy is observed in absence of toxicity.
- Example 19
- Example 9 Method A tagged with sulforhodamine dye. Post treatment the cells were evaluated for fluorescence. This fluorescence results for selective uptake of the formulation by the alveolar macrophages.
- Example 9 Method A The microparticles of formulation of Example 9 Method A were selectively taken up by the alveolar macrophages starting from 1 -hour post treatment.
- the dye shows gradual saturation in intensity at 3 hours. This is indicative of active uptake and a saturation point of the uptake.
- the mycobacteria reside and survive in the alveolar macrophages, hence it is very critical to ensure that the drug reaches the macrophages.
- By the designed microparticle formulation of Example 9 Method A it is evident that not only is compound of formula I reaching the macrophages but is being actively taken up by them, which is desired for the therapy to be successful in vivo.
- Example 9 Method A The Formulation of Example 9 Method A is actively taken up (gradual increase in the compound concentration) and metabolized by the macrophages (decrease in the compound concentration) as evident from the values in table 12.
- the free drug (compound of formula I) does not show active uptake (evident from the saturated concentrations of the free drug).
- Compound of formula I when developed as a lipid based microparticle formulation is actively taken up by the alveolar macrophages, which are the target for treatment.
- the therapy has the potential to actively reach the target and relevant cells.
- the assay was done as reported in The AAPS Journal, 2005, 7 (1 ), E20-E41 .
- Example 9 Method A A pilot in vivo lung deposition study was carried out as per the reference mentioned. Guinea pigs were divided in three groups. Group 1 received formulation of Example 9 Method A, group 2 received unformulated compound of formula I and group 3 was untreated (na ' ive group). 10 mg/kg of the formulation was aerosolized and the animals were allowed to breathe passively. Following administration of the formulation of Example 9 Method A the animals were sacrificed at 30 minutes time point. The lungs were collected and analyzed by HPLC. HPLC conditions are shown in Table 13. HPLC System Waters Alliance HPLC
- Example 9 Method A On nebulization, the unformulated compound of formula I was unable to reach the lungs.
- the formulation of Example 9 Method A was able to reach the lungs and retain for 24 hours and also exhibit compound of formula I after chronic daily exposure for 5 days.
- the capability of the lungs to retain the compound of formula I as formulation (formulation of Example 9 Method A) for five days can be used as five days of nebulization as a therapeutic regimen.
- the assay was done as reported in The AAPS Journal, 2005, 7 (1 ), E20-E41 .
- Example 9 Method A On nebulization, the unformulated compound of formula I was unable to reach the lungs.
- the formulation of Example 9 Method A was able to reach the lungs and the amount of compound of formula I absorbed by the lungs increased as the dose was doubled in a day.
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Abstract
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US13/813,470 US8697653B2 (en) | 2010-08-05 | 2011-08-04 | Microparticle formulation for pulmonary drug delivery of anti infective molecule for treatment of infectious diseases |
JP2013522337A JP2013532722A (en) | 2010-08-05 | 2011-08-04 | Particulate preparation for transpulmonary drug delivery of anti-infective molecules for treatment of infectious diseases |
IN329MUN2013 IN2013MN00329A (en) | 2010-08-05 | 2011-08-04 | |
KR1020137005739A KR20130109106A (en) | 2010-08-05 | 2011-08-04 | Microparticle formulation for pulmonary drug delivery of anti-infective molecule for treatment of infectious diseases |
BR112013002641A BR112013002641A2 (en) | 2010-08-05 | 2011-08-04 | formulation of microparticles for administration of anti-infective molecule pulmonary drugs for the treatment of infectious diseases |
CN201180043763.9A CN103442694B (en) | 2010-08-05 | 2011-08-04 | The infection molecule microparticle formulation of the pulmonary administration for the treatment of infectious disease |
CA2807357A CA2807357A1 (en) | 2010-08-05 | 2011-08-04 | Microparticle formulation for pulmonary drug delivery of anti-infective molecule for treatment of infectious diseases |
MX2013001325A MX2013001325A (en) | 2010-08-05 | 2011-08-04 | Microparticle formulation for pulmonary drug delivery of anti-infective molecule for treatment of infectious diseases. |
AU2011287205A AU2011287205A1 (en) | 2010-08-05 | 2011-08-04 | Microparticle formulation for pulmonary drug delivery of anti-infective molecule for treatment of infectious diseases |
RU2013109384/15A RU2013109384A (en) | 2010-08-05 | 2011-08-04 | COMPOSITION OF MICROPARTICLES FOR DELIVERY OF A MEDICINE FOR ANTI-INFECTIOUS MOLECULE FOR TREATMENT OF INFECTIOUS DISEASES |
EP11757941.7A EP2600842A1 (en) | 2010-08-05 | 2011-08-04 | Microparticle formulation for pulmonary drug delivery of anti-infective molecule for treatment of infectious diseases |
ZA2013/01662A ZA201301662B (en) | 2010-08-05 | 2013-03-05 | Microparticle formulation for pulmonary drug delivery of anti-infective molecule for treatment of infectious diseases |
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US37091610P | 2010-08-05 | 2010-08-05 | |
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US (1) | US8697653B2 (en) |
EP (1) | EP2600842A1 (en) |
JP (1) | JP2013532722A (en) |
KR (1) | KR20130109106A (en) |
CN (1) | CN103442694B (en) |
AU (1) | AU2011287205A1 (en) |
BR (1) | BR112013002641A2 (en) |
CA (1) | CA2807357A1 (en) |
IN (1) | IN2013MN00329A (en) |
MX (1) | MX2013001325A (en) |
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WO2015107482A1 (en) * | 2014-01-17 | 2015-07-23 | Piramal Enterprises Limited | Pharmaceutical combination for treatment of tuberculosis |
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US10335374B2 (en) | 2014-12-04 | 2019-07-02 | University System of Georgia, Valdosta State University | Tablet composition for anti-tuberculosis antibiotics |
CN109827875A (en) * | 2019-04-10 | 2019-05-31 | 上海市食品药品检验所 | A kind of device and method for measuring sucking preparation dissolution rate |
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WO2011027290A1 (en) | 2009-09-02 | 2011-03-10 | Piramal Life Sciences Limited | Antibiotic compounds |
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SE8601457D0 (en) * | 1986-04-01 | 1986-04-01 | Draco Ab | COMPOSITIONS OF LIPOSOMES AND B? 712 RECEPTOR ACTIVE SUBSTANCES FOR INHALATION |
TW497974B (en) * | 1996-07-03 | 2002-08-11 | Res Dev Foundation | High dose liposomal aerosol formulations |
CN100358494C (en) * | 1998-11-12 | 2008-01-02 | 弗兰克G·皮尔基威克兹 | Inhalation system |
US20030224039A1 (en) * | 2002-03-05 | 2003-12-04 | Transave, Inc. | Methods for entrapment of bioactive agent in a liposome or lipid complex |
ES2435197T3 (en) * | 2007-01-10 | 2013-12-16 | Board Of Regents, The University Of Texas System | Improved administration of immunosuppressive drug compositions for pulmonary administration |
-
2011
- 2011-08-04 RU RU2013109384/15A patent/RU2013109384A/en not_active Application Discontinuation
- 2011-08-04 AU AU2011287205A patent/AU2011287205A1/en not_active Abandoned
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- 2011-08-04 EP EP11757941.7A patent/EP2600842A1/en not_active Withdrawn
- 2011-08-04 JP JP2013522337A patent/JP2013532722A/en active Pending
- 2011-08-04 US US13/813,470 patent/US8697653B2/en active Active
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US4877561A (en) | 1986-04-02 | 1989-10-31 | Takeda Chemical Industries, Ltd. | Method of producing liposome |
WO2001054693A1 (en) * | 2000-01-31 | 2001-08-02 | Eisai Co., Ltd. | Use of thiostrepton as an anti-mycobacterial agent |
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Cited By (1)
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WO2015107482A1 (en) * | 2014-01-17 | 2015-07-23 | Piramal Enterprises Limited | Pharmaceutical combination for treatment of tuberculosis |
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AU2011287205A1 (en) | 2013-03-07 |
EP2600842A1 (en) | 2013-06-12 |
IN2013MN00329A (en) | 2015-05-29 |
CN103442694A (en) | 2013-12-11 |
JP2013532722A (en) | 2013-08-19 |
CA2807357A1 (en) | 2012-02-09 |
US20130125879A1 (en) | 2013-05-23 |
KR20130109106A (en) | 2013-10-07 |
US8697653B2 (en) | 2014-04-15 |
MX2013001325A (en) | 2013-10-28 |
TW201208716A (en) | 2012-03-01 |
CN103442694B (en) | 2015-09-09 |
RU2013109384A (en) | 2014-09-10 |
BR112013002641A2 (en) | 2016-06-07 |
ZA201301662B (en) | 2014-08-27 |
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