Biodegradable microbicidal vaginal barrier device

Details Biodegradable microbicidal vaginal barrier device Biodegradable microbicidal vaginal barrier device

2002-03-05

2003-07-22

Azpuru, Carlos A. (Department: 1615)

Drug, bio-affecting and body treating compositions

Preparations characterized by special physical form

Implant or insert

C424S431000, C424S432000, C424S434000, C424S435000, C424S436000, C424S443000, C424S494000

Reexamination Certificate

active

06596297

ABSTRACT:

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention concerns a biodegradable vaginal barrier device. More particularly, the present invention concerns a bio-erodible microbicidal vaginal sponge made from hydroxypropylmethylcellulose phthalate and/or cellulose acetate phthalate.
2. Background Information
Applicants have previously reported that cellulose acetate phthalate (“CAP”) and hydroxypropylmethylcellulose phthalate (“HPMCP”) prevent infection by the human immunodeficiency virus type 1 (HIV-1). Additional studies showed that CAP also blocked infection by several herpesviruses (Neurath, A. R., Strick, N., Li, Y.-Y., Jiang, S., “Design of a ‘Microbicide’ for Prevention of Sexually Transmitted Diseases Using ‘Inactive’ Pharmaceutical Excipients”,
Biologicals,
27, 11-21, (1999); U.S. Pat. No. 5,985,313; U.S. Pat. No. 6,165,493). CAP formulated into creams was shown to inactivate HIV-1, several herpesviruses as well as nonviral sexually transmitted disease (STD) pathogens (Neurath, A. R., Strick, N., Li, Y. -Y., Jiang, S., “Design of a ‘Microbicide’ for Prevention of Sexually Transmitted Diseases Using ‘Inactive’ Pharmaceutical Excipients”,
Biologicals,
27, 11-21, (1999); U.S. Pat. No. 5,985,313). The formulated CAP also inactivated bacteria associated with bacterial vaginosis (Neurath, A. R., Li, Y.-Y., Mandeville R., Richard, L., “In vitro Activity of a Cellulose Acetate Phthalate Topical Cream Against Organisms Associated with Bacterial Vaginosis”,
J. Antimicrob. Chemother.,
45, 713-714). Results of experiments in animal models indicated that CAP formulations prevented vaginal infections by the simian immunodeficiency virus (SIV) of macaques and by herpesvirus type 2 (HSV-2) of mice (In press: Manson, K. H., Wyand, M. S., Miller, C., Neurath, A. R., “The Effects of a Cellulose Acetate Phthalate Topical Cream on Vaginal Transmission of SIV in Rhesus Monkeys”,
Antimicrobial Agents & Chemotherapy;
Guotoku, T., Aurelian, L., Neurath, A. R., “Cellulose Acetate Phthalate (CAP): An ‘Inactive’ Pharmaceutical Excipient With Antiviral Activity in the Mouse Model of Genital Herpesvirus Infection”,
Antiviral Chemistry & Chemotherapy,
10, 327-332). Cumulatively these results indicate that formulations of CAP represent preferred microbicides for prevention of sexual transmission of a variety of STD pathogens.
To minimize the probability of conception, as well as of sexual transmission of HIV-1 and other STD pathogens, it appears critical to combine chemical and mechanical barriers (Shihata, A., “The Clinical Application of Basic Anatomy & Physiology in Microbicide Development”,
Microbicides
2000, Mar. 13-16, 2000, p. 29). The combinations of mechanical and chemical barriers in use at this time are based on solid mechanical devices combined with added detergents, Nonoxynol-9 (“N-9”) and other ingredients. Examples of such devices are as follows: Protectaid™ sponge (Axcan Ltd.), the Today Sponge™ (Allendale Pharmaceuticals, Inc., Allendale, N.J.) and the FemCap™ (Shihata, A. A., “The FemCap: A New Contraceptive Choice”,
Eur. J. Contracept. Reprod. Health Care,
3(3), pp. 160-166, (1998)). The disadvantage of these devices is that they have to be removed after use and either discarded (sponges), contributing to waste disposal problems, or cleaned for reuse (FemCap™), an impractical alternative for developing countries with scarce clean water supplies. Another disadvantage of these devices is the use of N-9 as a chemical barrier, since N-9 has been shown recently to increase the risk of sexual transmission of HIV-1 instead of blocking it. For all these reasons, alternative devices without these disadvantages are needed.
To avoid one of the above problems, such as the necessity to remove the device after use, a bio-erodible contraceptive suppository also expected to have microbicidal properties, has been described by Britton, P. et al. (U.S. Pat. No. 5,863,553). The Britton et al. device disperses or dissolves after use and therefore does not need to be removed. However the Britton et al. device still has the following disadvantages: (1) it uses N-9 as an added ingredient to provide contraceptive or microbicidal activity and (2) the device uses gelatine as a major ingredient to assure mechanical stability and ease of insertion. Gelatine is generally an undesirable animal derived product, which may potentially transmit spongiform encephalopathies (i.e., mad cow disease, Creuzfeldt-Jakob-Disease). For this reason, gelatine derived from animals susceptible to spongiform encephalopathies is not recommended, if avoidable, for medicinal use.
Devices with built-in contraceptive and microbicidal activity were disclosed by T. H. Barrows in U.S. Pat. No. 4,360,013. The Barrows devices are based on acidic polymers providing a low pH expected to be lethal to viruses, microorganisms and semen. However one of the proposed materials, oxidized cellulose (Oxycel) is prohibitively expensive and is not rapidly biodegradable. The general disadvantage of the acidic polymers listed in U.S. Pat. No. 4,360,013 is that the acidic functionalities would be neutralized in the presence of semen/seminal fluid. The neutralized polymers lack antiviral or antimicrobial activity.
SUMMARY OF THE INVENTION
It is an object of the present invention to provide a biodegradable microbicidal vaginal barrier device.
It is a further object of the present invention to furnish a bio-erodible microbicidal device for the prevention of sexually transmitted diseases.
It is a still further object of the present invention to provide a biodegradable vaginal sponge with built-in microbicidal activity.
The present invention satisfies the above objects and provides further objects, aims and advantages.
The present invention thus concerns an intravaginal bio-erodible microbicidal barrier device comprising:
(a) at least one micronized compound selected from the group consisting of cellulose acetate phthalate and hydroxypropylmethylcellulose phthalate, and
(b) at least one water soluble or water dispersible cellulose compound selected from the group consisting of hydroxypropylmethylcellulose, methylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxyethylmethylcellulose, hydroxyethylethylcellulose and hydroxypropylethylcellulose.
The cellulose acetate phthalate can be contained in an “AQUATERIC” composition which also contains poloxamers and aceylated monoglycerides.
The present invention also concerns an intravaginal bio-erodible microbicidal barrier device comprising:
(a) at least one microbicidal compound selected from the group consisting of cellulose acetate phthalate and hydroxymethylcellulose phthalate, and
(b) at least one pectin.
The present invention is also directed to an intravaginal bio-erodible microbicidal barrier device comprising:
(a) at least one micronized compound selected from the group consisting of cellulose acetate phthalate and hydroxypropylmethylcellulose phthalate, and
(b)(i) at least one water soluble or water dispersible cellulose compound selected from the group consisting of hydroxypropylmethylcellulose, methylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxyethylmethylcellulose, hydroxyethylethylcellulose and hydroxypropylethylcellulose and (ii) at least one pectin.
The present invention also relates to a method of making an intravaginal bio-erodible microbicidal barrier device comprising:
(a) providing at least one micronized compound selected from the group consisting of cellulose acetate phthalate and hydroxypropylmethylcellulose phthalate;
(b) adding to the at least one micronized compound, an aqueous solution of at least one water soluble or water dispersible cellulose compound selected from the group consisting of hydroxypropylmethylcellulose, methylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxyethylmethylcellulose, hydroxyethylethylcellulose and hydroxypropylethylcellulose, to form a suspension;
(c) foaming the suspension from step (b) to form a foam;
(d) disposing the foam from step (c) into a mold and freezing the foam to for

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