COMPOSITION FOR TOPICAL TREATMENT OF MIXED VAGINAL INFECTIONS
A pharmaceutical composition comprises (a) an antibacterial agent in an antibacterially effective amount, illustratively comprising clindamycin or a pharmaceutically acceptable salt or ester thereof; and (b) an antifungal agent in an antifungally effective amount, illustratively comprising butoconazole or a pharmaceutically acceptable salt or ester thereof. The composition is adapted for application in a unit dose amount to a vulvovaginal surface and has at least one nonlipoidal internal phase and at least one lipoidal external phase that is bioadhesive to the vulvovaginal surface. The composition is useful for administration to a vulvovaginal surface to treat a mixed bacterial vaginosis and vulvovaginal candidiasis infection.
1 . A pharmaceutical composition comprising:
(a) an antibacterially effective amount of clindamycin or a pharmaceutically acceptable salt or ester thereof;
(b) an antifungally effective amount of butoconazole or a pharmaceutically acceptable salt thereof; and
(c) polyethylene glycol-30 (PEG-30) dipolyhydroxystearate as an emulsifying agent; the composition being adapted for application to a vulvovaginal surface and having at least one nonlipoidal internal phase and at least one lipoidal external phase that is bioadhesive to the vulvovaginal surface.
2 . The composition of claim 1 , wherein the vulvovaginal surface to which the composition is adapted for application is a vaginal mucosal surface.
3 . The composition of claim 2 , wherein upon application of the composition to the vaginal mucosal surface the clindamycin or pharmaceutically acceptable salt or ester thereof and the butoconazole or pharmaceutically acceptable salt thereof each have a release period of about 3 hours to about 10 days.
4 . The composition of claim 3 , wherein upon application of the composition to the vaginal mucosal surface the clindamycin or pharmaceutically acceptable salt or ester thereof and the butoconazole or pharmaceutically acceptable salt thereof each have a release period of about 12 hours to about 10 days.
5 . The composition of claim 3 , wherein at least one of the clindamycin or pharmaceutically acceptable salt or ester thereof and the butoconazole or pharmaceutically acceptable salt thereof exhibits, by 1 day after administration, about 2% to about 25% release; by 2 days after administration, about 15% to about 50% release; by 3 days after administration, about 25% to about 75% release; and by 4 days after administration, about 45% to 100% release.
6 . The composition of claim 2 in a form of a vaginal cream.
7 . The composition of claim 6 , wherein the clindamycin or salt or ester thereof is present in a clindamycin equivalent amount of about 0.5% to about 6% by weight.
8 . The composition of claim 6 , wherein the clindamycin or salt or ester thereof is present in a clindamycin equivalent amount of about 1% to about 3% by weight.
9 . The composition of claim 6 , wherein the butoconazole or salt thereof is present in a butoconazole nitrate equivalent amount of about 0.5% to about 6% by weight.
10 . The composition of claim 6 , wherein the butoconazole or salt thereof is present in a butoconazole nitrate equivalent amount of about 1% to about 3% by weight.
11 . The composition of claim 6 , wherein the clindamycin or pharmaceutically acceptable salt or ester thereof comprises clindamycin phosphate and the butoconazole or pharmaceutically acceptable salt thereof comprises butoconazole nitrate.
12 . The composition of claim 1 , wherein the internal phase is acid buffered to an internal pH of about 2.0 to about 6.0.
13 . The composition of claim 1 , wherein the internal phase is acid buffered to an internal pH of about 4.0 to about 5.0.
14 . The composition of claim 1 , said composition being in a form of a vaginal cream comprising clindamycin phosphate in a clindamycin equivalent amount of about 2% by weight, and butoconazole nitrate in an amount of about 2% by weight; the composition having (i) at least one nonlipoidal internal phase; and (ii) at least one lipoidal external phase that is bioadhesive to a vaginal mucosal surface; wherein the internal phase comprises clindamycin phosphate and butoconazole nitrate.
15 . A vaginal antibacterial and antifungal delivery system comprising the composition of claim 6 and an applicator.
16 . The delivery system of claim 15 , wherein the applicator is disposable.
17 . The delivery system of claim 15 , wherein the applicator is prefilled with a unit dose amount of the composition.
18 . The delivery system of claim 17 , wherein the unit dose amount of the composition is about 1 to about 10 g.
19 . The delivery system of claim 17 , wherein the unit dose amount of the composition is about 3 to about 6 g.
20 . A method for treating a mixed bacterial vaginosis and vulvovaginal candidiasis infection, the method comprising administering to a vulvovaginal surface a pharmaceutical composition comprising:
(a) an antibacterially effective amount of clindamycin or a pharmaceutically acceptable salt or ester thereof;
(b) an antifungally effective amount of butoconazole or a pharmaceutically acceptable salt thereof; and
(c) polyethylene glycol-30 (PEG-30) dipolyhydroxystearate as an emulsifying agent; wherein the composition has at least one nonlipoidal internal phase and at least one lipoidal external phase that is bioadhesive to the vulvovaginal surface.
21 . The method of claim 20 , wherein:
(a) the clindamycin or pharmaceutically acceptable salt or ester thereof is present in a clindamycin equivalent amount of about 0.5% to about 6% by weight; and
(b) the butoconazole or pharmaceutically acceptable salt thereof is present in a butoconazole nitrate equivalent amount of about 0.5% to about 6% by weight.
22 . The method of claim 20 , wherein the vulvovaginal surface to which the composition is administered is a vaginal mucosal surface.
23 . The method of claim 22 wherein the composition is applied in a single dosage amount effective to provide an acceptable clinical response.
24 . The method of claim 23 , wherein the single dosage amount is about 1 to about 10 g.
25 . The method of claim 20 , comprising administering to a vaginal mucosal surface a single dosage amount of about 5 g of a vaginal cream composition comprising clindamycin phosphate in a clindamycin equivalent amount of about 2% by weight, and butoconazole nitrate in an amount of about 2% by weight; the vaginal cream composition having (i) at least one nonlipoidal internal phase; and (ii) at least one lipoidal external phase that is bioadhesive to the vaginal mucosal surface; wherein the internal phase comprises clindamycin phosphate and butoconazole nitrate.