NZ619707B2 - Sustained release formulations for delivery of proteins to the eye and methods of preparing same - Google Patents
Sustained release formulations for delivery of proteins to the eye and methods of preparing same Download PDFInfo
- Publication number
- NZ619707B2 NZ619707B2 NZ619707A NZ61970712A NZ619707B2 NZ 619707 B2 NZ619707 B2 NZ 619707B2 NZ 619707 A NZ619707 A NZ 619707A NZ 61970712 A NZ61970712 A NZ 61970712A NZ 619707 B2 NZ619707 B2 NZ 619707B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- tocopherol
- tri
- citrate
- lactide
- formulation
- Prior art date
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- 230000002459 sustained Effects 0.000 title claims abstract description 66
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- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/39541—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against normal tissues, cells
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- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/14—Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
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- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/20—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing sulfur, e.g. dimethyl sulfoxide [DMSO], docusate, sodium lauryl sulfate or aminosulfonic acids
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- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/34—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
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- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
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Abstract
Provided are liquid sustained release pharmaceutical formulations for delivery of active pharmaceutical ingredients to the eye. The formulations are particularly suitable for delivering proteins to the eye such as bovine gamma globulin. The formulations comprise at least one liquid biodegradable non-polymeric excipient, such as acetyl triethyl citrate (ATEC) or dimethyl sulfoxide (DMSO), and at least one biodegradable, biocompatible poly(D,L-lactide) (PLA) and/or poly(D,L-lactide-co-glycolide) (PLGA) polymer, wherein the ratio of non-polymeric excipient: polymer is about 90:10 to about 99:1. Further provided is the use of at least one biodegradable, biocompatible poly(D,L-lactide) (PLA) and/or poly(D,L-lactide-co-glycolide) (PLGA) polymer and at least one liquid biodegradable non-polymeric excipient in the manufacture of a medicament for treating eye disorders and other diseases such as cancer. -polymeric excipient, such as acetyl triethyl citrate (ATEC) or dimethyl sulfoxide (DMSO), and at least one biodegradable, biocompatible poly(D,L-lactide) (PLA) and/or poly(D,L-lactide-co-glycolide) (PLGA) polymer, wherein the ratio of non-polymeric excipient: polymer is about 90:10 to about 99:1. Further provided is the use of at least one biodegradable, biocompatible poly(D,L-lactide) (PLA) and/or poly(D,L-lactide-co-glycolide) (PLGA) polymer and at least one liquid biodegradable non-polymeric excipient in the manufacture of a medicament for treating eye disorders and other diseases such as cancer.
Description
SUSTAINED RELEASE FORMULATIONS FOR DELIVERY OF PROTEINS
TO THE EYE AND METHODS OF PREPARING SAME
RELATED APPLICATION
The present application claims priority benefit of U.S. Patent Application Ser.
No. 61/495,672, filed June 10, 2011, and incorporated fully herein.
FIELD OF THE INVENTION
This invention relates generally to biocompatible and biodegradable injectable
pharmaceutical formulations comprising therapeutic proteins, useful in the treatment of maladies
of the eye.
BACKGROUND
Present modes of drug delivery such as topical application, oral delivery, and
intramuscular, intravenous and subcutaneous injection may result in high and low blood
concentrations and/or shortened half-life in the blood. In some cases, achieving therapeutic
efficacy with these standard administrations requires large doses of medications that may result
in toxic side effects. The technologies relating to controlled drug release have been attempted in
an effort to circumvent some of the pitfalls of conventional therapy. Their aims are to deliver
medications on a continuous and sustained manner. Additionally, local control drug release
applications are site or organ specific. There remains a need for a more economical, practical,
and efficient way of producing and manufacturing drug delivery systems that could be used
locally or systemically, in solid, semi-solid, or liquid formulations. In particular, formulations
for sustained release in the eye have been developed, yet there is a need for improvement to
enhance sustained release of biologics-based medicaments in the eye.
SUMMARY
In one aspect the present invention relates to a pharmaceutical formulation for
injection into the eye for the sustained release of a therapeutic protein comprising:
a therapeutic protein,
at least one liquid, biodegradable, biocompatible non-polymeric excipient selected from
the group consisting of benzyl benzoate; esters of benzoic acid with straight, branched, or cyclic
chain aliphatic alcohols having one to twenty carbon atoms wherein one of the hydrogen atoms
on the aliphatic chain is replaced with a hydroxyl group; dimethyl sulfoxide; dimethyl sulfone;
dimethyl sulfozide; mono, di, and tri esters of O-acetylcitric acid or O-propionylcitric acid or O-
butyrylcitric acid with C to C straight and branched chain aliphatic alcohols; the mono, di, and
1 10
tri esters of citric acid with C to C straight and branched chain aliphatic alcohols; triethyl
1 10
citrate; acetyl triethyl citrate; tri-n-butyl citrate; acetyl tri-n-butyl citrate; acetyl tri-n-hexyl
citrate; butyryl tri-n-hexyl citrate; citric acid ethers; d-alpha-tocopherol; d,l-alpha-tocopherol; d-
beta-tocopherol; d,l-beta-tocopherol; d-eta-tocopherol; d,l-eta-tocopherol; acetate,
hemisuccinate, nicotinate, and succinate-PEG ester forms the preceding tocopherols; tocopheryl
acetate; tocotrienol isomers; tocotrienol esters; and
at least one biodegradable, biocompatible poly(D,L-lactide) (PLA) and/or poly(D,L-
lactide-co-glycolide) (PLGA) polymer;
wherein the wt% ratio of non-polymeric excipient:polymer is about 90:10 to 99:1,
inclusive;
wherein upon injection the formulation maintains its monolithic integrity and liquid
state; and
wherein the formulation releases the therapeutic protein for a period of at least
about 14 days..
In another aspect the present invention relates to the use of a therapeutic
protein,
at least one liquid, biodegradable, biocompatible non-polymeric excipient selected from the
group consisting of benzyl benzoate; esters of benzoic acid with straight, branched, or cyclic
chain aliphatic alcohols having one to twenty carbon atoms wherein one of the hydrogen atoms
on the aliphatic chain is replaced with a hydroxyl group; dimethyl sulfoxide; dimethyl sulfone;
dimethyl sulfozide; mono, di, and tri esters of O-acetylcitric acid or O-propionylcitric acid or O-
butyrylcitric acid with C to C straight and branched chain aliphatic alcohols; the mono, di, and
1 10
tri esters of citric acid with C to C straight and branched chain aliphatic alcohols; triethyl
1 10
citrate; acetyl triethyl citrate; tri-n-butyl citrate; acetyl tri-n-butyl citrate; acetyl tri-n-hexyl
citrate; butyryl tri-n-hexyl citrate; citric acid ethers; d-alpha-tocopherol; d,l-alpha-tocopherol; d-
beta-tocopherol; d,l-beta-tocopherol; d-eta-tocopherol; d,l-eta-tocopherol; acetate,
hemisuccinate, nicotinate, and succinate-PEG ester forms the preceding tocopherols; tocopheryl
acetate; tocotrienol isomers; tocotrienol esters; and
at least one biodegradable, biocompatible poly(d,l-lactide) (PLA) and/or poly(d,l-lactide-co-
glycolide) (PLGA) polymer in the manufacture of a medicament to treat an affliction of the eye.
In another aspect the use of a therapeutic protein, at least one liquid,
biodegradable, biocompatible non-polymeric excipient selected from the group consisting of
benzyl benzoate; esters of benzoic acid with straight, branched, or cyclic chain aliphatic alcohols
having one to twenty carbon atoms wherein one of the hydrogen atoms on the aliphatic chain is
replaced with a hydroxyl group; dimethyl sulfoxide; dimethyl sulfone; dimethyl sulfozide;
mono, di, and tri esters of O-acetylcitric acid or O-propionylcitric acid or O-butyrylcitric acid
with C to C straight and branched chain aliphatic alcohols; the mono, di, and tri esters of citric
1 10
acid with C to C straight and branched chain aliphatic alcohols; triethyl citrate; acetyl triethyl
1 10
citrate; tri-n-butyl citrate; acetyl tri-n-butyl citrate; acetyl tri-n-hexyl citrate; butyryl tri-n-hexyl
citrate; citric acid ethers; d-alpha-tocopherol; d,l-alpha-tocopherol; d-beta-tocopherol; d,l-beta-
tocopherol; d-eta-tocopherol; d,l-eta-tocopherol; acetate, hemisuccinate, nicotinate, and
succinate-PEG ester forms the preceding tocopherols; tocopheryl acetate; tocotrienol isomers;
tocotrienol esters; and
at least one biodegradable, biocompatible poly(d,l-lactide) (PLA) and/or poly(d,l-lactide-co-
glycolide) (PLGA) polymer in the manufacture of a medicament to treat angiogenesis, bone
resorption, restenosis, diabetic retinopathy, or tumor growth..
In another aspect the present invention relates to a syringeable ophthalmic
formulation comprising:
a pharmaceutically active protein in a therapeutically effective amount for those in need
thereof;
an amount of non-polymeric excipient selected from the group consisting of benzyl
benzoate; esters of benzoic acid with straight, branched, or cyclic chain aliphatic alcohols having
one to twenty carbon atoms wherein one of the hydrogen atoms on the aliphatic chain is replaced
with a hydroxyl group; dimethyl sulfoxide, dimethyl sulfone; dimethyl sulfozide; mono, di, and
tri esters of O-acetylcitric acid or O-propionylcitric acid or O-butyrylcitric acid with C to C
1 10
straight and branched chain aliphatic alcohols; the mono, di, and tri esters of citric acid with C
to C straight and branched chain aliphatic alcohols; triethyl citrate; acetyl triethyl citrate; tri-n-
butyl citrate; acetyl tri-n-butyl citrate; acetyl tri-n-hexyl citrate; butyryl tri-n-hexyl citrate; and/or
citric acid ethers; d-alpha-tocopherol; d,l-alpha-tocopherol; d-beta-tocopherol; d,l-beta-
tocopherol; d-eta-tocopherol; d,l-eta-tocopherol; acetate, hemisuccinate, nicotinate, and
succinate-PEG ester forms of the preceding tocopherols; tocopheryl acetate; tocotrienol isomers;
tocotrienol esters;
an amount of at least one biodegradable, biocompatible poly(D, L- lactide) (PLA) or
poly(D,L-lactide-co-glycolide) (PLGA) polymer;
wherein the wt% ratio of non-polymeric excipient:polymer ranges from 90:10 to 99:1,
inclusive; and
wherein said pharmaceutically active protein is solubilized or dispersed in
said formulation.
Certain statements that appear below are broader than what appears in the
statements of the invention above. These statements are provided in the interests of providing
the reader with a better understanding of the invention and its practice. The reader is directed to
the accompanying claim set which defines the scope of the invention.
Disclosed herein are liquid sustained release formulations in which the kinetics of
active agent release can be controlled using relatively simple formulations comprising at least
one non-polymeric liquid excipient (for example, a citrate ester, a benzyl benzoate, or dimethyl
sulfone), and a small amount (e.g., less than 10% ± 1%) of a poly(D, L- lactide) (PLA) or
poly(D,L-lactide-co-glycolide) (PLGA) polymer. Additionally, when combined with the non-
polymeric excipients described herein, PLA and PLGA with or without acid end groups produce
different release kinetics. Further, PLGA with different percentages of lactide and glycolide
moieties (e.g., lactide:glycolide of 50:50; 65:35; 75:25; or 85:15) yield different sustained
release kinetics. Thus, these excipients provide for a variety of formulations from which the
release rate of active agent can be sustained for a desired length of time.
Embodiments described herein provide for a pharmaceutical formulation for
injection into the eye for the sustained release of an active agent comprising: at least one active
agent; at least one biodegradable, biocompatible, non-polymeric, liquid excipient selected from
the group consisting of benzyl benzoate (BB); esters of benzoic acid with straight, branched, or
cyclic chain aliphatic alcohols having one to twenty carbon atoms wherein one of the hydrogen
atoms on the aliphatic chain is replaced with a hydroxyl group (e.g., such alcohols as methanol,
ethanol, n-propanol, i-propanol, n-butanol, i-butanol, s-butanol, t-butanol, n-pentanol,
i-pentanol, neo-pentanol, n-hexanol, cyclohexanol, n-heptanol, n-octonol, n-nonanol, n-decanol,
and the like); dimethyl sulfide; dimethyl sulfoxide; dimethyl sulfone; dimethyl sulfozide; mono,
di, and tri esters of O-acetylcitric acid or O-propionylcitric acid or O-butyrylcitric acid with C
to C straight and branched chain aliphatic alcohols; the mono, di, and tri esters of citric acid
with C to C straight and branched chain aliphatic alcohols; triethyl citrate (TEC); triethyl-O-
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acetyl citrate (TEAC); acetyl triethyl citrate (ATEC); tri-n-butyl citrate; acetyl tri-n-butyl citrate;
acetyl tri-n-hexyl citrate; butyryl tri-n-hexyl citrate; or citric acid ethers; d-alpha-tocopherol;
d,l-alpha-tocopherol; d-beta-tocopherol; d,l-beta-tocopherol; d-eta-tocopherol; and d,l-eta-
tocopherol (including acetate, hemisuccinate, nicotinate, and succinate-PEG ester forms of each
of the foregoing); tocopheryl acetate; tocotrienol isomers, tocotrienol esters; and at least one
biodegradable, biocompatible poly(D, L- lactide) (PLA) or poly(D,L-lactide-co-glycolide)
(PLGA) polymer; wherein the ratio of non-polymeric excipient:polymeric excipient is
about 90:10 to about 99:1, inclusive; such that upon initial injection the composition maintains
its monolithic integrity in a liquid state; and wherein the composition releases the active agent
for a period of at least about 14 days.
The formulations of the present embodiments can be colorless or nearly colorless;
can be injectable through a small needle; and can be used in the eye. The formulations of the
present embodiments are particularly advantageous for the sustained release of proteins, such as
antibodies, in the eye.
In a specific embodiment, the formulation is a unit dosage formulation of
about 5 µl to about 100 µl that can injected into the subconjunctiva, periocular space, retrobulbar
in the orbit, episclera, intracornea, intrasclera, anterior chamber, anterior segment, posterior
chamber, posterior segment, vitreous cavity, subretinal space, suprachorodial segment, or
intraretinal area of the eye.
DESCRIPTION OF THE DRAWINGS
Figure 1 shows in vitro release profiles of dexamethasone released from three
different formulations: 6% Dexamethasone/95% ATEC (■); 6% Dexamethasone/94%
(5% RG752H/95% ATEC) (□); 6% Dexamethasone/94% (5% RG502/95% ATEC) (♦).
Figure 2 shows in vitro release profiles of dexamethasone released from four
different formulations, each consisting of 6% dexamethasone in the balance of either ATEC (■);
% R202H/95% ATEC (♦); 5% R203H/95% ATEC (●); or 5% R203S/95% ATEC (▲).
Figure 3 presents in vitro release profiles of dexamethasone released from four
different formulations, each consisting of 6% dexamethasone in the balance of either ATEC (■);
% RG502H/ATEC (□); 5% RG502/ATEC (♦); or 5% RG505/ATEC (▲).
Figure 4 depicts in vitro release profiles of dexamethasone released from four
different formulations, each consisting of 6% dexamethasone in the balance of either ATEC (■);
1.25% PLGA (85:15 lactide:glycolide)/ATEC (♦); 5% RG502H (50:50
lactide:glycolide)/ATEC (□); or 5% RG756S (75:25 lactide:glycolide)/ATEC (●).
Figure 5 shows in vitro release profiles of bovine gamma globulin (BGG)
released from a formulation of 1% BGG in 5% PLGA RG502H/ATEC at either ambient
temperature () or 37°C (∆). N=10.
Figure 6 shows in vitro release profiles of BGG released from formulations of
either 1% BGG in 5% PLGA RG502H/ATEC (∆) or 1% BGG in 5% PLGA RG502/ATEC (),
both formulations maintained at 37°C.
Figure 7 shows the 37°C in vitro release profile of BGG released from a
formulation of 1% BGG in excipient consisting of 5% PLGA RG502 in
ATEC/BB/DMSO (50:38:12).
Figure 8 compares in vitro release profiles of BGG released from a formulation
of 1% BGG in 5% PLGA RG502 in ATEC placed in infinite sink conditions either immediately
after preparation (), or after storage for about 2 4 hours at 4°C (∆).
Figure 9 shows in vitro release profiles of BGG released at 37°C from
formulations of 1% BGG and either 5% RG502/TEC (); 5% RG502H/TEC (∆);
% RG653H/TEC (◊); or 5% RG752H/TEC (○).
Figure 10 compares in vitro release profiles of BGG (ave. %, y-axis) released
from a formulation of 3% BGG in an excipient consisting of either 1.7% PLGA RG502 in
BB:DMSO 75:25 (♦); or 5% PLGA RG502 in BB:DMSO 75:25 (■). x-axis, days; N=4.
Figure 11 shows an in vitro release profile of BGG released (ave. %, y-axis) from
a formulation of 1.5% BGG in 5% PLGA RG502 in ATEC/BB/DMSO (50:38:12). x-axis, days.
Figure 12 compares in vitro release profiles of BGG (ave. %, y-axis) released
from a 10 µL aliquot of a formulation consisting of 1% BGG in either 7.5% PLGA RG502 in
ATEC (♦); 5% PLGA RG502 in ATEC (■); or 7.1% PLGA RG502 in 87.5% ATEC and
4.4% DMSO (●). Formulations had been stored at room temperature for 8 days prior to being
placed in infinite sink release conditions. x-axis, days.
Figure 13 presents several in vitro release profiles of BGG (ave. %, y-axis)
released from a 10 µL aliquot of a formulation consisting of 1% BGG in either 1.25% PLGA
(85:15 lactide:glycolide) (balance ATEC in each formulation) (□); 5% PLGA RG653H (●);
% PLGA RG752H (◊); 5% PLGA RG756S (○); 10% PLGA RG502H (■); 5% PLGA
RG502H; or 5% PLGA RG502. x-axis, days.
Figure 14 compares release profiles of BGG (ave. %, y-axis) released from two
different size aliquots of formulations consisting of either 1% BGG or 3% BGG in an excipient
consisting of 5% PLGA RG502 ATEC:EA 98:2. Aliquots were 10 µL 1% BGG (♦); 50 µL
1% BGG (■); 10 µL 3% BGG (▲); 50 µL 3% BGG (○). N=3; x-axis, days.
Figure 15 shows in vivo release of BGG from formulations consisting of
either 1% or 3% BGG in an excipient consisting of 5% PLGA R502 in ATEC. A unit dose
of 50 µL was injected into the posterior segment of rabbit eyes.
DETAILED DESCRIPTION
It should be understood that this invention is not limited to the particular
methodology, protocols, and reagents, etc., described herein and as such may vary. The
terminology used herein is for the purpose of describing particular embodiments only, and is not
intended to limit the scope of the present invention, which is defined solely by the claims.
As used herein and in the claims, the singular forms include the plural reference
and vice versa unless the context clearly indicates otherwise. Other than in the operating
examples, or where otherwise indicated, all numbers expressing quantities of ingredients or
reaction conditions used herein should be understood as modified in all instances by the term
“about,” which unless otherwise indicated, in relation to percent values, means ± 1%.
All patents and other publications identified are expressly incorporated herein by
reference for the purpose of describing and disclosing, for example, the methodologies described
in such publications that might be used in connection with the present invention. These
publications are provided solely for their disclosure prior to the filing date of the present
application. Nothing in this regard should be construed as an admission that the inventors are not
entitled to antedate such disclosure by virtue of prior invention or for any other reason. All
statements as to the date or representation as to the contents of these documents is based on the
information available to the applicants and does not constitute any admission as to the
correctness of the dates or contents of these documents.
Unless defined otherwise, all technical and scientific terms used herein have the
same meaning as those commonly understood to one of ordinary skill in the art to which this
invention pertains. Although any known methods, devices, and materials may be used in the
practice or testing of the invention, the methods, devices, and materials in this regard are
described herein.
Described herein are sustained release formulations in which the kinetics of
active agent release can be controlled using relatively simple formulations comprising an
excipient (for example, a citrate ester, a benzyl benzoate, dimethyl sulfone), and a small amount
(e.g., less than about 10%) of a poly(D, L- lactide) (PLA) or poly(D,L-lactide-co-glycolide)
(PLGA) polymer. Additionally, PLA and PLGA with and/or without acid end groups produce
different release kinetics. Further, PLGA with different percentages of lactide and glycolide
moieties (e.g., lactide:glycolide of 50:50; 65:35; 75:25; or 85:15) yield different sustained
release kinetics. Thus, these excipients provide for the design of a variety of formulations from
which the release rate of active agent can be sustained for the desired length of time.
The non-polymeric excipients of the present embodiments include benzyl
benzoate; esters of benzoic acid with straight, branched, or cyclic chain aliphatic alcohols having
one to twenty carbon atoms wherein one of the hydrogen atoms on the aliphatic chain is replaced
with a hydroxyl group (e.g., such alcohols as methanol, ethanol, n-propanol, i-propanol, n-
butanol, i-butanol, s-butanol, t-butanol, n-pentanol, i-pentanol, neo-pentanol, n-hexanol,
cyclohexanol, n-heptanol, n-octonol, n-nonanol, n-decanol, and the like); dimethyl sulfoxide,
dimethyl sulfone; dimethyl sulfozide; mono, di, and tri esters of O-acetylcitric acid or
O-propionylcitric acid or O-butyrylcitric acid with C to C straight and branched chain
1 10
aliphatic alcohols; the mono, di, and tri esters of citric acid with C to C straight and branched
1 10
chain aliphatic alcohols; triethyl citrate; acetyl triethyl citrate; tri-n-butyl citrate; acetyl tri-n-
butyl citrate; acetyl tri-n-hexyl citrate; butyryl tri-n-hexyl citrate; and/or citric acid ethers; d-
alpha-tocopherol; d,l-alpha-tocopherol; d-beta-tocopherol; d,l-beta-tocopherol; d-eta-tocopherol;
and d,l-eta-tocopherol (including acetate, hemisuccinate, nicotinate, and succinate-PEG ester
forms of each of the foregoing); tocopheryl acetate; tocotrienol isomers, and their esters.
See, e.g., U.S. Patents No. 7,906,136, No. 7,560,120, and No. 6,960,346; U.S. Patent
Pub. 2011/0111006. The non-polymeric excipients of the present embodiments biocompatible in
that they are non-toxic and non-irritating, are physically and chemically stable, and do not
compromise the stability of a active agent with which they are formulated.
Poly(glycolic acid) (PGA), Poly(lactic acid) (PLA) and their copolymers have
been researched for a wide range of applications. These biodegradable aliphatic polyesters have
proven biocompatibility and versatile biodegradation properties depending on their molecular
weight and chemical compositions: PLA/PGA are biodegradable polyesters that degrade in the
body by simple hydrolysis of the ester backbone to non-harmful and non-toxic compounds. The
in vivo degradation products are either excreted by the kidneys or eliminated as carbon dioxide
and water through well-known biochemical pathways. Typically, active agent has been
entrapped in solid poly(D,L-lactide-co-glycolide)-based (PLGA-based) matrices in which
release of the agent is achieved by bioerosion of the polymer followed by exposure of previously
entrapped agent. See, e.g., U.S. Patents No. 6,369,116; No. 6,699,493; No. 6,726,918;
No. 7,048,946.
Some PLGA-based implants have been made by dissolving polymer in a
biocompatible polar aprotic solvent that is miscible to dispersible in body fluid such that, upon
administration, the solvent dissipates to produce a solid implant (in situ forming implants). In
order for this to occur, the polymer component is present at ≥30 wt.% and the solvent is present
at ≤70 wt.%. See U.S. Patent No. 6,773,714.
In contrast to other polymer-based drug delivery systems, the present
embodiments provide for formulations in which the liquid state of the polymer is maintained,
and the monolithic integrity of the unit dose is maintained following injection. More
specifically, when syringed carefully (e.g., into the eye), the formulations of the present
embodiments maintain monolithic integrity in a liquid state, in which the biocompatible,
biodegradable excipients are maintained and gradually dissolve over time as the active agent is
delivered. The embodiments described herein are injectable liquid formulations in which the
polymer is present ≤10 wt.% (± 1%) of the formulation. For example, the polymer:non-polymer
excipient may be prepared in a ratio of polymer excipient:non-polymer excipient(s) that is may
be 1:99 to 10:90 (wt.%), inclusive; for example, 5:95 PLGA:TEC (5 wt.% PLGA and 95 wt.%
citrate ester). The excipient portion of the formulation can be prepared and then mixed with the
active agent. For example, a 5%PLGA in benzyl benzoate (BB) is prepared (e.g., by stirring),
and then mixed with immunoglobulin at 2 wt.% (i.e., 2 mg immunoglobulin and 98 mg
PLGA:benzyl benzoate).
The formulations of the present invention are injectable through a relatively small
gauge syringe needle, for example, a 25, 27, 28, or 30 gauge, or smaller, needle. The unit dose of
the formulation for administration in the eye is minute, generally about 5 µL to about 100 µL,
inclusive, yet a single unit dose delivers a sustained, therapeutic concentration of active agent for
at least 14 days. The formulations of the present invention can be colorless or nearly colorless,
which can be advantageous for use in the eye.
The formulations of the present invention are also advantageous for use in the eye
because, although liquid, they maintain monolithic integrity when placed in the eye, which is to
say they form a contiguous shape and do not disintegrate or disperse into smaller particles or
precipitants in the eye. Once administered into the eye, the physician can observe the placement
and size of the formulation in the eye, although the subject is not aware of its presence (i.e., the
dose of formulation does not obstruct vision). Typically, as long as the formulation is still visible
to the physician it is still delivering active agent. This physical characterization is also useful in
preparing formulations according to the embodiments herein, because a particular mixture of
excipients can readily be prepared and placed in a saline or other fluid environment that mimics
conditions in the eye, and observed for maintenance of monolithic integrity.
Regarding polymer excipients that may be used in concert with the non-
polymeric excipients of the present embodiments, PLGA is a polymer that, when mixed with
particular excipients as described herein, is suitable for sustained release formulations. PLGA
can have different amounts of lactide and glycolide moieties (e.g., lactide:glycolide of 50:50;
65:35; 75:25; or 85:15), which affects the sustained release kinetics of the formulation. For
example, PLGA 50/50 is a polymer with a 50:50 molar composition of D,L-lactic and glycolic
acid in the PLGA chain. See, e.g., U.S. Patent No. 4,728,721. There are generally three types of
PLGA end-groups functions: (i) free carboxylic acid group, (ii) ester terminated group, and (iii)
alkyl ester group. Polymers “capped” with ester and alkyl ester groups have different polarity
and typically show longer degradation lifetimes than the free carboxylic analogs. Additionally,
when used as a solid matrix (e.g., implants or nanoparticles) PLGA polymers having high
molecular weight typically release agent more slowly that PLGAs of lower molecular weight.
See Gasper et al., 52 J. Control Release 53 (1998).
According to the present embodiments, various PLA, PGA and PLGA polymers
can be mixed in liquid excipients as a small percentage (typically about 10% or less) of the
volume of the excipient portion of a pharmaceutical formulation, and extend the sustained
release profile of agent compared with the release from the liquid excipient alone. Although the
use such polymers in solid sustained release formulation has been reported (for example, solid
polymer implants, microspheres, or nanospheres), that the addition of a relatively small amount
of liquid polymer to a non-polymeric sustained release liquid excipient would modulate the
sustained release profile of the non-polymeric excipient is unexpected. Thus, polymer can be
used in the formulations of the present invention at about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%,
9%, or about 10% (wt/wt), or any fraction thereof, inclusive.
Without being bound by theory, in contrast to current PLGA sustained release
compositions and formulations in which active agent is entrapped in the pores of a solid matrix
PLGA, in the present embodiments the polymer remains liquid and acts in concert with the
liquid, non-polymeric excipient, associating with the liquid excipient and active agent in a loose
floating web that disassociates as lactide residues leave the polymer.
The formulations described herein provide for the sustained release of agents
such as therapeutic proteins for at least 14 days. This is understood by those of skill in the art to
be distinguished from therapeutic effect, which may last for a longer period (or shorter period)
than the period over which the therapeutic protein is released from the particular formulation.
Release can be sustained for at least 14 days or longer, such as 21 days, 28 days, 35 days, 42
days, 49 days, etc., up to and including 150 days or longer. In this regard, the days or weeks of
sustained release can be interpreted and extrapolated from the Figures by one of ordinary skill in
the art and are incorporated into the present written description.
The active agents which may be used in the present embodiments include, but are
not limited to, anti-glaucoma agents, analgesics, anesthetics, narcotics, angiostatic steroids, anti-
inflammatory steroids, angiogenesis inhibitors, nonsteroidal anti-inflammatories, anti-infective
agents, anti-fungals, anti-malarials, anti-tuberculosis agents, anti-virals, alpha androgenergic
agonists, beta adrenergic blocking agents, carbonic anhydrase inhibitors, mast cell stabilizers,
miotics, prostaglandins, antihistamines, antimicrotubule agents, antineoplastic agents,
antiapoptotics, aldose reductase inhibitors, antihypertensives, antioxidants, growth hormone
antagonists, vitrectomy agents, adenosine receptor antagonists, adenosine delaminate inhibitor,
glycosylation antagonists, anti-aging peptides, topoisemerase inhibitors, anti-metabolites,
alkylating agents, antiandrigens, anti-oestogens, oncogene activation inhibitors, telomerase
inhibitors, antibodies or portions thereof, antisense oligonucleotides, fusion proteins, luteinizing
hormone releasing hormones agonists, gonadotropin releasing hormone agonists, tyrosine kinase
inhibitors, epidermal growth factor inhibitors, ribonucleotide reductase inhibitors, cytotoxins,
IL2 therapeutics, neurotensin antagonists, peripheral sigma ligands, endothelin ETA/receptor
antagonists, antihyperglycemics, anti-chromatin modifying enzymes, obesity management
agents, anemia therapeutics, emesis therapeutics, neutropaenia therapeutics, tumor-induced
hypercalcaemia therapeutics, blood anticoagulants, anti-proliferatives, immunosuppressive
agents, tissue repair agents, psychotherapeutic agents, Aptamers (Eyetech), Lucentis
(Genentech), RNA inhibitors, insulin, human insulin, GLP-1, and Byetta (exenatide, Amylin).
The formulations of the present invention are particularly advantageous for the
sustained release of proteins, in particular, proteinaceous ligands such as antibodies. Antibodies,
as used herein means intact immunoglobulin molecules as well as portions, fragments, peptides,
analogs or derivatives thereof such as, for example, Fab, Fab', F(ab') , Fv, CDR regions,
paratopes, or any portion or peptide sequence of an antibody that is capable of binding an
antigen or epitope, and includes monovalent antibodies, divalent antibodies, polyclonal
antibodies, monoclonal antibodies, chimeric antibodies, fully humanized antibodies,
recombinant antibodies, and monoclonal antibodies produced by transgenic animals. An
antibody is said to be “capable of binding” a molecule if it is capable of specifically reacting
with the molecule to thereby bind the molecule to the antibody.
Ocular disorders that may be treated using formulations according to the present
embodiments include diabetic retinopathies, proliferative retinopathies, retinal detachment, toxic
retinopathies, retinal vascular diseases, retinal degenerations, vascular anomalies, age-related
macular degeneration, infectious diseases, inflammatory diseases, ocular ischemia, pregnancy-
related disorders, retinal tumors, choroidal tumors, choroidal disorders, vitreous disorders,
trauma, cataract complications, dry eye, inflammatory optic neuropathies, and other
acquired disorders.
A “disorder” is any condition that would benefit from treatment with, for
example, a sustained release agent. This includes chronic and acute disorders or diseases
including those pathological conditions which predispose the subject to the disorder in question.
For example, ocular-related disorders in which the vasculature of the eye is
damaged or insufficiently regulated. Neovascularization is associated with exudative age-related
macular degeneration, diabetic retinopathy, corneal neovascularization, choroidal
neovascularization, neovascular glaucoma, cyclitis, Hippel-Lindau Disease, retinopathy of
prematurity, pterygium, histoplasmosis, iris neovascularization, macular edema, glaucoma-
associated neovascularization, and the like. Disorders associated with both neovascular and
atrophic components, such as age-related macular degeneration and diabetic retinopathy, are
particularly difficult to treat due to the emergence of a wide variety of complications. Atrophic
complications include, for instance, the formation of drusen and basal laminar deposits,
irregularity of retinal pigmentation, and accumulation of lipofuscin granules.
The formulations of the present invention can be used for the therapeutic or
prophylactic treatment of the eye(s) of a subject. “Therapeutic” refers to the amelioration of the
ocular-related disorder, itself, and the protection, in whole or in part, against further ocular-
related disease, such as ocular neovascularization or age-related macular degeneration.
“Prophylactic” refers to the protection, in whole or in part, against ocular-related disorders, such
as ocular neovascularization or age-related macular degeneration. One of ordinary skill in the art
will appreciate that any degree of protection from, or amelioration of, an ocular-related disorder
is beneficial to a subject. The invention is particularly advantageous in that a therapeutic agent
can be directly applied to affected areas of the eye without the harmful side effects of
systemic therapies.
Therapeutic proteins that can be formulated according to the present
embodiments include cytokines, inhibitors of angiogenesis, neurotrophic agents, steroids,
enzymes (e.g., hyaluronidase), and antibodies.
Example inhibitors of angiogenesis include aflibercept (a fusion protein of key
binding domains of human VEGFR-1 and -2 combined with a human IgG Fc fragment), pigment
epithelium-derived factor (PEDF), anti-VEGF antibody or portion thereof (such as ranibizumab
or bevacizumab) angiostatin, vasculostatin, endostatin, platelet factor 4, heparinase, interferons,
tissue inhibitor of metalloproteinase 3, and tyrosine kinase inhibitors, and the like. Such factors
may prevent the growth of new blood vessels, promote vessel maturation, inhibit permeability of
blood vessels, inhibit the migration of endothelial cells, and the like. See, e.g., WO 02/22176.
Another class of therapeutic proteins are neurotrophic factors, which include
neuropoietic cytokines, neurotrophins, and the fibroblast growth factors. Ciliary neurotrophic
factor (CNTF) is an exemplary of neuropoietic cytokine, that promotes the survival of ciliary
ganglionic neurons and supports certain neurons that are NGF-responsive. Neurotrophins
include, for example, brain-derived neurotrophic factor and nerve growth factor, perhaps the
best characterized neurotrophic factor. Other neurotrophic factors include, for example,
transforming growth factors, glial cell-line derived neurotrophic factor, neurotrophin 3,
neurotrophin 4/5, and interleukin 1-β. Neuronotrophic factors enhance neuronal survival, and
may reverse degradation of neurons. PEDF is an example protein exhibiting anti-angiogenic and
neurotrophic activities.
Further regarding antibodies, antibody-based immunosuppressive therapies
include anti-IL-2R antibodies (e.g., basiliximab or daclizumab) and anti-CD52 antibodies (e.g.,
alemtuzumab), abatacept and the affinity-matured belatacept (antibody-based constructs
combining the extracellular part of the immunomodulatory CTLA4 receptor with a human IgG
Fc region), antithymocyte globulin, muronomab (anti-CD3 antibody), or infliximab (anti-
TNF-α). See Thiel et al., 23 Eye 1962 (2009). Additionally, lerdelimumab (anti-TGFb2) human
monoclonal antibody has been used in subjects undergoing surgery for glaucoma and cataract.
One of ordinary skill in the art will appreciate that particular therapeutic protein
can be modified or truncated (e.g., by recombinant or fragmentation approaches), and retain
biological activity. As such, active portions of various proteins (e.g., those portions of anti-
angiogenic proteins having biological activity sufficient to inhibit angiogenesis) are also suitable
for use in the present formulations.
Cytokines can also be formulated according to the embodiments hwerein. A
“cytokine” refers to any of a diverse group of soluble proteins and peptides which act as humoral
regulators at nano- to picomolar concentrations and which, either under normal or pathological
conditions, modulate the functional activities of individual cells and tissues. These proteins also
mediate interactions between cells directly and regulate processes taking place in the
extracellular environment. Examples of cytokines include, but are not limited to interleukins
IL-1, IL-2, IL-4, IL-5, IL-6, IL-7, IL-10, IL-12, IL-15, IL-18; granulocyte-macrophage colony-
stimulating factor (GM-CSF); granulocyte colony-stimulating factor (G-CSF); interferons
including interferon-alpha (IFN-α), interferon-beta (IFN-β), and interferon-gamma (IFN-γ);
tumor necrosis factor (TNF), transforming growth factor-beta (TGF-β); FLT-3 ligand; and
CD40 ligand.
In one embodiment described herein, the active agent is a monoclonal antibody.
In a specific example formulation, about 2% (wt.) antibody was suspended in a solution of
about 5% PLGA (lactide:glycolide 50:50, MW range 7,000-17,000, alkyl ester end group)
(Evonik Röhm GmbH, Darmstadt, Germany; Sigma-Aldrich, St. Louis, MO), in acetyl triethyl
citrate (ATEC). Antibody release from this formulation was sustained for at least 14 days at
bioactive and therapeutic levels. In another embodiment, the active agent is a monoclonal
antibody suspended in a formulation consisting of about 5% PLGA (lactide:glycolide 65:35,
MW range 24,000-38,000, free carboxylic acid end group) in ATEC. Antibody release was
sustained at a low level, exhibiting near zero-order kinetics, for at least 14 days, and antibody
maintained antigen binding specificity. In yet another embodiment, the active agent is a
monoclonal antibody suspended in a formulation consisting of about 6% PLGA
(lactide:glycolide 75:25, MW range 4,000-15,000, free carboxylic acid end group) in ATEC.
Antibody release was sustained at a low level for at least 14 days, and antibody maintained
antigen binding specificity throughout this time period.
In another embodiment, recombinant monoclonal IgG antibody was formulated
in 5% PLGA in ATEC or, as control, PBS. Rabbits were administered 50 µL doses containing
1 mg IgG, by bilateral intravitreal injection. Rabbits were humanely euthanized on days 1, 7, 14,
and 28 post-administration, and concentrations of test IgG in vitreous humor (pellet and
supernatant fractions), retina, choroid, and plasma were compared. Time-points were tested in
duplicate or triplicate and averaged. In the plasma, the concentration of IgG from the PBS
formulation rose rapidly until it peaked at day 7; whereas the concentration of IgG from the
PLGA/ATEC formulation remained lower and leveled off by day 28. In the vitreous, the
concentration of IgG from the PBS formulation decreased over time in all tissues; whereas the
concentration of IgG from the PLGA/ATEC formulation remained steady in the pellet fraction,
and steadily increased in the supernatant fraction; the concentration of IgG from the
PLGA/ATEC formulation was higher in both vitreous fractions on day 28 compared with
concentration of IgG from the PBS formulation. In the retina and choroid, the concentration of
IgG from the PBS formulation spiked initially, then decreased over time. In contrast, the
concentration of IgG from the PLGA/ATEC formulation increased steadily over time, and was
higher at day 28 in both the retina and choroid compared with the PBS formulation. IgG was
delivered to the eye tissues for at least 14 days (i.e., 28 days).
“Treat,” “treatment,” “treating,” or “amelioration” refer to therapeutic treatments,
wherein the object is to reverse, alleviate, ameliorate, inhibit, slow down or stop the progression
or severity of a condition associated with, a disease or disorder. The term “treating” includes
reducing or alleviating at least one adverse effect or symptom of a condition, disease or disorder
associated with a disorder of the eye, such as, ocular edema. Treatment is generally “effective” if
one or more symptoms or clinical markers are reduced. Alternatively, treatment is “effective” if
the progression of a disease is reduced or halted. That is, “treatment” includes not just the
improvement of symptoms or markers, but also a cessation of at least slowing of progress or
worsening of symptoms that would be expected in absence of treatment. Beneficial or desired
clinical results include, but are not limited to, alleviation of one or more symptom(s),
diminishment of extent of disease, stabilized (i.e., not worsening) state of disease, delay or
slowing of disease progression, amelioration or palliation of the disease state, and remission
(whether partial or total), whether detectable or undetectable. The term “treatment” of a disease
also includes providing relief from the symptoms or side-effects of the disease (including
palliative treatment).
In general, the goal of treatment is reducing the size of a tumor or level of an
antigen, or inhibiting the activity of a target, as measured using a suitable in vitro, cellular or in
vivo assay. In particular, decreasing the biological activity of a target, antigen or tumor, as
measured using a suitable in vitro, cellular or in vivo assay (which will usually depend on the
target involved), by at least 5%, 10%, 25%, 50%, 60%, 70%, 80%, or 90%, or 100%, inclusive,
as compared with an equivalent untreated control. A decrease refers to a statistically significant
decrease. For the avoidance of doubt, a decrease will be at least 5% relative to a reference, such
as at least 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or more, up to and including
100%, inclusive. Reduce or inhibit can refer to, for example, the symptoms of the disorder being
treated, such as the a reduction in ocular pressure or lessening of retinal edema.
An “effective amount” as used herein is any amount that is sufficient either to
promote the occurrence of a desired outcome or condition, or to reduce or inhibit the occurrence
of an undesired outcome or condition. In some instances a desired outcome or condition is an
ideal that represents one end of a spectrum of possible outcomes or conditions. In such instances
an effective amount is any amount associated with an outcome or condition that is closer to the
desired ideal than would be achieved or observed without the effective amount. Thus, an
effective amount promotes the occurrence of a desired outcome or condition, but it need not
achieve an ultimate endpoint.
Additional agents and therapies can be combined with the administration of the
formulations of the present embodiments. Thus, although the formulations of the invention and
the methods described herein in certain instances may be useful for replacing existing surgical
procedures or drug therapies, the present invention is also useful in improving the efficacy of
existing therapies for treating such conditions. Accordingly, combination therapy may be used to
treat the subjects that are undergoing or that will undergo a treatment for, inter alia, eye disease
or tumor/cancer. For example, the agents described herein can be administered in conjunction
with anti-microbial agents or anti-proliferative agents. The agents described herein also can be
administered in conjunction with other immunotherapies, such as with antigens, adjuvants,
immunomodulators, or passive immune therapy with antibodies. In some embodiments the
method described herein further involves administering to the subject an anti-cancer
medicament. The agents described herein also can be administered in conjunction with nondrug
treatments, such as surgery, radiation therapy or chemotherapy. Alternatively, and as indicated
by medical condition, the treatment with sustained release therapeutic agents as described herein
further involves administering to the subject an antibacterial, antiviral, antimycobial, antifungal,
antiparasitic, or other antiinfective medicament. The other therapy may be administered before,
concurrent with, or after treatment with the agents described herein. There may also be a delay
of several hours, days and in some instances weeks between the administration of the different
treatments, such that the agents described herein may be administered before or after the other
treatment.
As will be understood by those of ordinary skill in the art, the appropriate doses
of agents formulated as described herein, with or without additional agents, will be generally
around those already employed in clinical therapies, e.g., where the chemotherapeutics are
administered alone or in combination with other chemotherapeutics. Variation in dosage will
likely occur depending on the condition being treated. The physician administering treatment
will be able to determine the appropriate dose for the individual subject.
Pharmaceutical formulations may be conveniently presented in unit dosage form
and may be prepared by any of the methods well known in the art of pharmacy. All methods
include the step of bringing the active agent, e.g., the therapeutic protein, into association with
the excipients described herein. In general, the formulations are prepared by uniformly and
intimately bringing the agent into association with a liquid excipient containing ≤10% polymer.
Formulations for injection may be presented in unit dosage form, e.g., in ampoules or in
multi-dose containers
The invention is described further in the following non-limiting examples.
EXAMPLES
Example 1. Formulations comprising dexamethasone in ATEC with or without PLGA
In general, formulations of dexamethasone in acetyl triethyl citrate (ATEC) were
prepared as follows. Poly(D,L–lactide–co-glycolide) (PLGA) or poly(D,L–lactide) (PLA)
(Evonik Röhm GmbH, Darmstadt, Germany; Sigma-Aldrich, St. Louis, MO) and ATEC were
weighed and placed in a 20 mL scintillation vial. The typical lot size was10 gram total weight,
e.g., for a formulation of 5% RG502H (lactide:glycolide 50:50, MW range 7,000-17,000, free
carboxylic acid end group) in ATEC: 500 mg of RG502H and 9500 mg of ATEC were weighed,
mixed, and stirred in the scintillation vial with a magnetic stir bar. The mixture was stirred at
ambient temperature until total dissolution of the polymer. This generally takes several hours to
overnight stirring, depending on the polymer used. Once the polymer/ATEC had been mixed to
a clear, colorless solution, the desired amount of dexamethasone and the polymer/ATEC
solution were weighed, e.g., to make a 6% wt. dexamethasone in 5% RG502H/ATEC, 120 mg
of dexamethasone and 1880 mg of 5% RG502H/ATEC were weighed, to make a total of 2 g of
the formulation.
For sample preparation, the dexamethasone/polymer/ATEC suspension was
vortexed vigorously for 5-10 sec. An aliquot of the formulation mixture was removed with a
mechanical pipet and loaded into a BD polypropylene Insulin syringe with a 28 gauge needle
(VWR Product #309300). The syringe containing the formulation was weighed (pre-injection
weight). A 10 µL aliquot of the formulation was injected into a 20 mL scintillation vial
containing 10 mL of 0.9% saline (“release medium”), forming a monolithic shape (e.g., a sphere
or “ball”) of the formulation at the bottom of the vial. Any excess saline on the syringe was
wiped off, and the syringe weighed again (post-injection weight). The actual amount of
formulation injected can be calculated by subtracting the post-injection weight from pre-
injection weight.
The samples were placed in a 37°C oven, and at each sampling day, 5 mL of the
release-medium was removed for analysis and replaced the with 5 mL of fresh release medium
to maintain a 10 mL total volume at all times (maintaining an “infinite sink”). The sampling
days were typically day 1, day 3 (or day 4), day 7, day 14, and weekly thereafter until all
dexamethasone had been released into the medium from the formulation “ball.”
All samples were analyzed by High Performance Liquid Chromatography
(HPLC) with the following conditions:
Column: Waters Nova-Pak, C18, 4 um, 150 mm x 3.9 mm
Mobile Phase: H O (H PO ), pH 2.5 – acetonitrile, gradient condition from (60:40) to
2 3 4
(10:90) in 9 min then returning back to (60:40)
Flow Rate: 0.5 mL/min
Detector: 240 nm
Sample volume: 10 µL
Standard Concentrations: 30 µg/mL, 60 µg/mL, and 120 µg/mL
Three formulations were compared, each having 6% dexamethasone in ATEC
(6% Dexamethasone/ATEC) either without or with 5% of either RG752H (Poly(D,L-lactide-co-
glycolide), lactide:glycolide 75:25, MW range 4,000-15,000, free carboxylic acid end group)
(6% Dexamethasone/5% RG752H/ATEC); or PLGA RG502 (Poly(D,L-lactide-co-glycolide),
lactide:glycolide 50:50, MW range 7,000-17,000, alkyl ester end group)
(6% Dexamethasone/5% RG502/ATEC).
To analyze in vitro release profiles, an aliquot of 10µL of each formulation was
injected into 10 mL 0.9% saline and incubated at 37ºC, then aliquots of 5mLwere exchanged
weekly (i.e., infinite sink) and sample was assayed for dexamethasone concentration by standard
HPLC method. The resulting sustained release profiles are shown in Figure 1. As can be seen
from the graph in Figure 1, 10 µl of the formulation of dexamethasone in ATEC sustained the
release of dexamethasone for at least 14 days; 10 µl of the formulation of dexamethasone in
ATEC/5%RG752 sustained the release of dexamethasone for at least 56 days; and 10 µl of the
formulation of dexamethasone in ATEC/5%RG502 sustained the release of dexamethasone for
at least 98 days.
Example 2. Formulations comprising dexamethasone in ATEC with/without PLA
Four formulations were compared, comprising dexamethasone in ATEC
(6% Dexamethasone/ATEC) without or with 5% of either R202H (Poly(D,L-lactide), MW
range 10,000-18,000, free carboxylic acid end group) (6% Dexamethasone/5% R202H/ATEC);
R203H (Poly(D,L-lactide), MW range18,000-28,000, free carboxylic acid end group)
(6% Dexamethasone/5% R203H/ATEC); or R203S (Poly(D,L-lactide),
MW range18,000-28,000, ester terminated) (6% Dexamethasone/5% R203S/ATEC).
A release profile was generated as in Example 1, and the resulting sustained
release profiles are shown in Figure 2. As can be seen from the graph in Figure 2, 10 µl of the
formulation of dexamethasone in ATEC sustained the release of dexamethasone for at least
14 days; 10 µl of the formulation of dexamethasone in ATEC/5%R202H sustained the release of
dexamethasone for at least 70 days; and 10 µl of the formulation of dexamethasone in
ATEC/5%R203H sustained the release of dexamethasone for at least 98 days; and 10 µl of the
formulation of dexamethasone in ATEC/5%R203S sustained the release of dexamethasone for at
least 154 days.
Example 3. Formulations comprising dexamethasone in ATEC with/without PLGA
Four formulations were compared, comprising dexamethasone in ATEC (6%
Dexamethasone/ATEC) without or with 5% of either PLGA RG502H (6% Dexamethasone/5%
RG502H/ATEC); PLGA RG502 (6% Dexamethasone/5% RG502/ATEC); or PLGA RG505
(Poly(D,L-lacide-co-glycolide, D,L-lactide:glycolide 50:50, MW ~80,000, alkyl ester end
group) (6% Dexamethasone/5% RG505/ATEC). A release profile was generated as in
Example 1, and the resulting sustained release profiles are shown in Figure 3.
As can be seen from the graph in Figure 3, 10 µl of the formulation of
dexamethasone in ATEC sustained the release of dexamethasone for at least 14 days; 10 µl of
the formulation of dexamethasone in ATEC/5%RG502H sustained the release of dexamethasone
for at least 49 days; 10 µl of the formulation of dexamethasone in ATEC/RG502H sustained the
release of dexamethasone for at least 98 days; and 10 µl of the formulation of dexamethasone in
ATEC/5%RG505 sustained the release of dexamethasone for at least 98 days, with slower
release at the outset of the analysis period.
Example 4. Formulations comprising dexamethasone, ATEC, and PLGA with different
lactide:glycolide ratios.
Four formulations were compared, comprising dexamethasone in ATEC
(6% Dexamethasone/ATEC) and dexamethasone in ATEC with PLGAs having different percent
of lactide and glycolide (i.e., lactide:glycolide ratios of 50:50; 75:25; or 85:15) (6%
Dexamethasone/5% RG502H (50:50)/ATEC); RG756S (Poly(D,L-lactide-co-glycolide), 75:25,
MW range 76,000-116,000, ester terminated) (6% Dexamethasone/5% RG756S (75:25)/ATEC);
PLGA (85:15) Poly(D,L-lactide-co-glycolide), lactide:glycolide (85:15),
MW Range 50,000-75,000 (6% Dexamethasone/1.25% PLGA(85:15)/ATEC).
A release profile was generated as in Example 1, and the resulting sustained
release profiles are shown in Figure 4. As can be seen in Figure 4, 10 µl of the formulation of
dexamethasone in ATEC sustained the release of dexamethasone for at least 14 days; 10 µl of
the formulation of dexamethasone in ATEC/PLGA (85:15) sustained the release of
dexamethasone for at least 42 days; 10 µl of the formulation of dexamethasone in ATEC/5%
RG502H (50:50) sustained the release of dexamethasone for at least 56 days; and 10 µl of the
formulation of dexamethasone in ATEC/5%RG756S (75:25) sustained the release of
dexamethasone for at least 84 days.
Example 5. Sustained release formulations of bovine gamma globulin (BGG)
A formulation of 1% BGG in 5% PLGA RG502H/ATEC was prepared. Briefly,
1% or 1.5% of fine, powdered γ–globulins from bovine blood (BGG, Cohn fraction II and III,
Sigma) were added to a solution of 5% PLGA in ATEC. The resulting suspensions were mixed
by vortexing and sonicating until even distribution was observed.
For in vitro sustained release analysis, 10 µL aliquots of the BGG formulation
were placed in a matrix of 10 ml 0.9% saline, 1% porcine albumin and 0.05% sodium azide, and
incubated at either ambient or 37°C. More specifically, a 20 mL glass release vial was weighed.
Then, a 10 µL droplet of the test formulation (suspension) was placed into the glass vial, the
total weight of vial and the formulation was measured, and the weight of the added formulation
(droplet) calculated. To the vial containing the droplet, 10 mL of release matrix was added. The
resulting vial containing the release matrix and the droplet at the bottom of the vial were
incubated at wither ambient or 37°C. At each time point, the vial was equilibrated to room
temperature, and 5 mL of the matrix solution was carefully withdrawn for BGG determination.
Then, 5 mL of the release matrix was added back to the 20 mL glass vial to maintain infinite
sink conditions, and the vial returned to incubation at 37°C. Sampling and replacement of matrix
were repeated at each time point.
BBG determination was performed using Bovine IgG ELISA Quantitation set
(Bethyl Laboratories, Inc., Montgomery, TX). BGG stock standard (1.00 mg/ml) was prepared
in 0.9% saline containing 1% PSA and 0.05% sodium azide and stored at +4°C for a month.
BGG working standards (in the range from 0 ng/mL to 500 ng/mL) were prepared freshly by
diluting the stock standard in the assay buffer (also used for sample dilutions). The BGG
concentrations were determined against standard calibration curve according to the ELISA
Protocol (Bethyl Laboratories, Inc). Figure 5 was generated. In this formulation, the release of
BGG was sustained for at least 16 days at 37°C, and for at least 60 days at ambient temperature.
Example 6. BGG release comparing PLGA RGA502H with PLGA RG502
Formulations of 1% BGG in 5% PLGA RG502H/ATEC and 1% BGG in 5%
PLGA RG502/ATEC were prepared as in Example 5. Figure 6 was generated, N=3. The results
indicated that BGG was released for at least 14 days from the RG502H/ATEC excipient, and at
least 49 days from the RG502/ATEC excipient.
Example 7. Sustained release of BGG in ATEC/BB/DMSO and 5% PLGA RG502
Formulations of 1% BGG in 5% PLGA RG502 in ATEC/BB/DMSO (50:38:12)
were prepared. Data was generated as in Example 5, and graphed and is shown in Figure 7, N=4.
As can be seen from the graph, BGG release was sustained for at least 60 days at 37°C.
In a similar embodiment, a formulation of 1.5% BGG in 5% PLGA RG502 in
ATEC/BB/DMSO (50:38:12) was prepared. When placed in test medium, the formulation
formed a monolithic, roughly flat, bolus on the bottom of the vial. An in vitro BGG release
profile was generated as shown in Figure 11. As can be seen from the data, BGG was still being
released into the media after 130 days.
Example 8. Comparison of fresh with stored formulation of BGG.
Formulations of 1% BGG in 5% PLGA RG502 in ATEC were prepared and
BGG release studied as in Example 5. One formulation was stored for about 24 hr at 4°C (Aged)
before being subjected to the release study. Figure 8 was generated, N=3. The formulations that
had been stored for about 24 hr at 4°C (Aged), exhibited slower in vitro release than did freshly
(Fresh) made formulations, but in both cases BGG release was sustained for at least 35 days.
Example 9. Sustained release of BGG from triethyl citrate (TEC) and various PLGAs
Formulations of 1% BGG in TEC and 5% PLGA RG502, RG502H, RG653H
(Poly(D,L-lactide-co-glycolide), 65:35, MW range 24,000-38,000, free carboxylic acid end
group), or RG752H (Poly(D,L-lactide-co-glycolide) 75:25, MW range 24,000-38,000, free
carboxylic acid end group) were prepared. Figure 9 was generated as in Example 5, N=3. In all
formulations, BGG release was sustained in vitro for at least 15 days, although the
TEC/RG752H formulation can be projected to sustain release for at least 23 days.
Example 10. Sustained release of BGG from PLGA/ATEC or PLGA/ATEC/DMSO.
Three formulations of BGG were prepared by mixing 1% BGG in either
% PLGA RG502 in ATEC; 7.5% PLGA RG502 in ATEC; or 7.1% PLGA RG502 in
87.5% ATEC and 4.4% DMSO. All formulations were stored at room temperature for 8 days
prior to being placed in infinite sink release conditions. When a 10 µL aliquot was placed in
infinite sink media, these formulations maintained a rather round monolith on the bottom of the
test vial. The results are shown in Figure 12. BGG was still being released from each
formulation at 51 days.
Example 11. Sustained release of BGG from PLGA/BB/DMSO formulations
Formulations of BGG were prepared by mixing 3% BGG in excipient mixtures
consisting of either 1.7% PLGA RG502 in BB:DMSO 75:25; or 5% PLGA RG502 in
BB:DMSO 70:25. Results of in vitro release are shown in Figure 10.
Example 12. Sustained release of BGG from PLGA/EA/ATEC formulations
Tocopherols provide for another sustained release vehicle with which release
rates can be modulated by addition of small amounts of PLGA. Formulations of BGG were
prepared by mixing either 1% BGG or 3% BGG in an excipient mixture consisting of 5% PLGA
RG502 ATEC:EA 98:2 (i.e. 98% wt ATEC and 2% wt tocopherol acetate). Aliquots of
either 10 µL or 50 µL were tested, in triplicate, for in vitro release of BGG, and results are
shown in Figure 14.
Example 13. In vivo sustained release of antibody in PLGA/ATEC formulations
Formulations consisting of either 3% BGG in saline or 1% or 3 % BGG in %5
RG502 and ATEC were prepared. A single unit dose of 50 µL was administered to the posterior
segment of rabbits, and the release of BGG measured thereafter. As can be seen from Figure 15,
BGG release from 3% BGG in saline was rapid and relatively short-lived in comparison with
BGG release from the PLGA/ATEC formulations, which provided for slow release for well
over 14 days. Indeed, these data support the conclusion that the present sustained release
formulations can release therapeutic doses of therapeutic proteins over long periods of time, and
could allow patients to enjoy several weeks or months between injections.
Modifications of the above described modes for carrying out the invention that
are obvious to those of ordinary skill in the surgical, pharmaceutical, or related arts are intended
to be within the scope of the appended claims.
The term “comprising” as used in this specification and claims means “consisting
at least in part of”. When interpreting statements in this specification, and claims which include
the term “comprising”, it is to be understood that other features that are additional to the features
prefaced by this term in each statement or claim may also be present. Related terms such as
“comprise” and “comprised” are to be interpreted in similar manner.
Claims (13)
1. A pharmaceutical formulation for injection into the eye for the sustained release of a therapeutic protein comprising: a therapeutic protein, at least one liquid, biodegradable, biocompatible non-polymeric excipient selected from the group consisting of benzyl benzoate; esters of benzoic acid with straight, branched, or cyclic chain aliphatic alcohols having one to twenty carbon atoms wherein one of the hydrogen atoms on the aliphatic chain is replaced with a hydroxyl group; dimethyl sulfoxide; dimethyl sulfone; dimethyl sulfozide; mono, di, and tri esters of O-acetylcitric acid or O-propionylcitric acid or O- butyrylcitric acid with C to C straight and branched chain aliphatic alcohols; the mono, di, and 1 10 tri esters of citric acid with C to C straight and branched chain aliphatic alcohols; triethyl 1 10 citrate; acetyl triethyl citrate; tri-n-butyl citrate; acetyl tri-n-butyl citrate; acetyl tri-n-hexyl citrate; butyryl tri-n-hexyl citrate; citric acid ethers; d-alpha-tocopherol; d,l-alpha-tocopherol; d- beta-tocopherol; d,l-beta-tocopherol; d-eta-tocopherol; d,l-eta-tocopherol; acetate, hemisuccinate, nicotinate, and succinate-PEG ester forms the preceding tocopherols; tocopheryl acetate; tocotrienol isomers; tocotrienol esters; and at least one biodegradable, biocompatible poly(D,L-lactide) (PLA) and/or poly(D,L- lactide-co-glycolide) (PLGA) polymer; wherein the wt% ratio of non-polymeric excipient:polymer is about 90:10 to 99:1, inclusive; wherein upon injection the formulation maintains its monolithic integrity and liquid state; and wherein the formulation releases the therapeutic protein for a period of at least about 14 days.
2. The pharmaceutical formulation of claim 1, wherein the straight, branched, or cyclic chain aliphatic alcohols are selected from the group consisting of methanol, ethanol, n-propanol, i-propanol, n-butanol, i-butanol, s-butanol, t-butanol, n-pentanol, i-pentanol, neo-pentanol, n- hexanol, cyclohexanol, n-heptanol, n-octonol, n-nonanol, and n-decanol.
3. The pharmaceutical formulation of claim 1 or claim 2, wherein the formulation is a unit dosage of about 5 µl to about 100 µl that can injected into the subconjunctiva, periocular space, retrobulbar in the orbit, episclera, intracornea, intrasclera, anterior chamber, anterior segment, posterior chamber, posterior segment, vitreous cavity, subretinal space, suprachorodial segment or intraretinal area of the eye.
4. The formulation of any one of claims 1 to 3, wherein the therapeutic protein is an antibody.
5. Use of a therapeutic protein, at least one liquid, biodegradable, biocompatible non-polymeric excipient selected from the group consisting of benzyl benzoate; esters of benzoic acid with straight, branched, or cyclic chain aliphatic alcohols having one to twenty carbon atoms wherein one of the hydrogen atoms on the aliphatic chain is replaced with a hydroxyl group; dimethyl sulfoxide; dimethyl sulfone; dimethyl sulfozide; mono, di, and tri esters of O-acetylcitric acid or O-propionylcitric acid or O- butyrylcitric acid with C to C straight and branched chain aliphatic alcohols; the mono, di, and 1 10 tri esters of citric acid with C to C straight and branched chain aliphatic alcohols; triethyl 1 10 citrate; acetyl triethyl citrate; tri-n-butyl citrate; acetyl tri-n-butyl citrate; acetyl tri-n-hexyl citrate; butyryl tri-n-hexyl citrate; citric acid ethers; d-alpha-tocopherol; d,l-alpha-tocopherol; d- beta-tocopherol; d,l-beta-tocopherol; d-eta-tocopherol; d,l-eta-tocopherol; acetate, hemisuccinate, nicotinate, and succinate-PEG ester forms the preceding tocopherols; tocopheryl acetate; tocotrienol isomers; tocotrienol esters; and at least one biodegradable, biocompatible poly(d,l-lactide) (PLA) and/or poly(d,l-lactide- co-glycolide) (PLGA) polymer in the manufacture of a medicament to treat an affliction of the eye.
6. Use of a therapeutic protein, at least one liquid, biodegradable, biocompatible non-polymeric excipient selected from the group consisting of benzyl benzoate; esters of benzoic acid with straight, branched, or cyclic chain aliphatic alcohols having one to twenty carbon atoms wherein one of the hydrogen atoms on the aliphatic chain is replaced with a hydroxyl group; dimethyl sulfoxide; dimethyl sulfone; dimethyl sulfozide; mono, di, and tri esters of O-acetylcitric acid or O-propionylcitric acid or O- butyrylcitric acid with C to C straight and branched chain aliphatic alcohols; the mono, di, and 1 10 tri esters of citric acid with C to C straight and branched chain aliphatic alcohols; triethyl 1 10 citrate; acetyl triethyl citrate; tri-n-butyl citrate; acetyl tri-n-butyl citrate; acetyl tri-n-hexyl citrate; butyryl tri-n-hexyl citrate; citric acid ethers; d-alpha-tocopherol; d,l-alpha-tocopherol; d- beta-tocopherol; d,l-beta-tocopherol; d-eta-tocopherol; d,l-eta-tocopherol; acetate, hemisuccinate, nicotinate, and succinate-PEG ester forms the preceding tocopherols; tocopheryl acetate; tocotrienol isomers; tocotrienol esters; and at least one biodegradable, biocompatible poly(d,l-lactide) (PLA) and/or poly(d,l-lactide- co-glycolide) (PLGA) polymer in the manufacture of a medicament to treat angiogenesis, bone resorption, restenosis, diabetic retinopathy, or tumor growth.
7. The use of claim 5 or claim 6, wherein the straight, branched, or cyclic chain aliphatic alcohols are selected from the group consisting of methanol, ethanol, n-propanol, i-propanol, n- butanol, i-butanol, s-butanol, t-butanol, n-pentanol, i-pentanol, neo-pentanol, n-hexanol, cyclohexanol, n-heptanol, n-octonol, n-nonanol, and n-decanol.
8. The use of any one of claims 5 to 7 where the medicament is in the form of a pharmaceutical formulation.
9. A syringeable ophthalmic formulation comprising: a pharmaceutically active protein in a therapeutically effective amount for those in need thereof; an amount of non-polymeric excipient selected from the group consisting of benzyl benzoate; esters of benzoic acid with straight, branched, or cyclic chain aliphatic alcohols having one to twenty carbon atoms wherein one of the hydrogen atoms on the aliphatic chain is replaced with a hydroxyl group; dimethyl sulfoxide, dimethyl sulfone; dimethyl sulfozide; mono, di, and tri esters of O-acetylcitric acid or O-propionylcitric acid or O-butyrylcitric acid with C to C 1 10 straight and branched chain aliphatic alcohols; the mono, di, and tri esters of citric acid with C to C straight and branched chain aliphatic alcohols; triethyl citrate; acetyl triethyl citrate; tri-n- butyl citrate; acetyl tri-n-butyl citrate; acetyl tri-n-hexyl citrate; butyryl tri-n-hexyl citrate; and/or citric acid ethers; d-alpha-tocopherol; d,l-alpha-tocopherol; d-beta-tocopherol; d,l-beta- tocopherol; d-eta-tocopherol; d,l-eta-tocopherol; acetate, hemisuccinate, nicotinate, and succinate-PEG ester forms of the preceding tocopherols; tocopheryl acetate; tocotrienol isomers; tocotrienol esters; an amount of at least one biodegradable, biocompatible poly(D, L- lactide) (PLA) or poly(D,L-lactide-co-glycolide) (PLGA) polymer; wherein the wt% ratio of non-polymeric excipient:polymer ranges from 90:10 to 99:1, inclusive; and wherein said pharmaceutically active protein is solubilized or dispersed in said formulation.
10. The syringeable ophthalmic formulation of claim 9, wherein the straight, branched, or cyclic chain aliphatic alcohols are selected from the group consisting of methanol, ethanol, n-propanol, i-propanol, n-butanol, i-butanol, s-butanol, t-butanol, n-pentanol, i-pentanol, neo-pentanol, n-hexanol, cyclohexanol, n-heptanol, n-octonol, n-nonanol, and n-decanol.
11. The formulation of any one of claims 1 to 4, 9 and 10, wherein the PLGA has a lactide:glycolide ratio of 50:50, MW range 7,000-17,000, and an alkyl ester end group.
12. A formulation as defined in any one of claims 1 to 4, 9 and 10 substantially as herein described with reference to any example thereof.
13. A use as defined in any one of claims 5 to 8 substantially as herein described with reference to any example thereof.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161495672P | 2011-06-10 | 2011-06-10 | |
US61/495,672 | 2011-06-10 | ||
PCT/US2012/041950 WO2013036309A2 (en) | 2011-06-10 | 2012-06-11 | Sustained release formulations for delivery of proteins to the eye and methods of preparing same |
Publications (2)
Publication Number | Publication Date |
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NZ619707A NZ619707A (en) | 2015-01-30 |
NZ619707B2 true NZ619707B2 (en) | 2015-05-01 |
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