Designed Chemical Intervention with Thiols for Prophylactic Contraception

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dc.contributor.author Sharma, Monika
dc.contributor.author Kumar, Lokesh
dc.contributor.author Jain, Ashish
dc.contributor.author Verma, Vikas
dc.contributor.author Sharma, Vikas
dc.contributor.author Kushwaha, Bhavana
dc.contributor.author Lal, Nand
dc.contributor.author Kumar, Lalit
dc.contributor.author Rawat, Tara
dc.contributor.author Dwivedi, A K
dc.contributor.author Maikhuri, J P
dc.contributor.author Sharma, V L
dc.contributor.author Gupta, Gopal
dc.date.accessioned 2013-07-05T06:50:00Z
dc.date.available 2013-07-05T06:50:00Z
dc.date.issued 2013
dc.identifier.citation PLoS ONE 8(6): e67365. en
dc.identifier.uri http://hdl.handle.net/123456789/1081
dc.description.abstract Unlike somatic cells, sperm have several-fold more available-thiols that are susceptible to redox-active agents. The present study explains the mechanism behind the instant sperm-immobilizing and trichomonacidal activities of pyrrolidinium pyrrolidine-1-carbodithioate (PPC), a novel thiol agent rationally created for prophylactic contraception by minor chemical modifications of some known thiol drugs. PPC, and its three derivatives (with potential active-site blocked by alkylation), were synthesized and evaluated against live human sperm and metronidazole-susceptible and resistant Trichomonas vaginalis, in vitro. Sperm hexokinase activity was evaluated by coupled enzyme assay. PPC irreversibly immobilized 100% human sperm in ,30 seconds and totally eliminated Trichomonas vaginalis more efficiently than nonoxynol-9 and metronidazole. It significantly inhibited (P,0.001) thiol-sensitive sperm hexokinase. However, the molecule completely lost all its biological activities once its thiol group was blocked by alkylation. PPC was subsequently formulated into a mucoadhesive vaginal film using GRaS excipients and evaluated for spermicidal and microbicidal activities (in vitro), and contraceptive efficacy in rabbits. PPC remained fully active in quick-dissolving, mucoadhesive vaginal-film formulation, and these PPC-films significantly reduced pregnancy and fertility rates in rabbits. The films released ,90% of PPC in simulated vaginal fluid (pH 4.2) at 37uC in 5 minutes, in vitro. We have thus discovered a common target (reactive thiols) on chieflyanaerobic, redox-sensitive cells like sperm and Trichomonas, which is susceptible to designed chemical interference for prophylactic contraception. The active thiol in PPC inactivates sperm and Trichomonas via interference with crucial sulfhydryl-disulfide based reactions, e.g. hexokinase activation in human sperm. In comparison to non-specific surfactant action of OTC spermicide nonoxynol-9, the action of thiol-active PPC is apparently much more specific, potent and safe. PPC presents a proof-of-concept for prophylactic contraception via manipulation of thiols in vagina for selective targeting of sperm and Trichomonas, and qualifies as a promising lead for the development of dually protective vaginal-contraceptive en
dc.format.extent 938339 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries C.D.R.I. Communication No. 8464 en
dc.subject Sulfhydryls en
dc.subject Hexokinase en
dc.subject Microbicidal spermicide en
dc.subject Trichomonas vaginalis en
dc.subject Contraceptive film en
dc.title Designed Chemical Intervention with Thiols for Prophylactic Contraception en
dc.type Article en


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