Vaginal Drug Absorption in Rhesus Monkeys I: Development of Methodology

Owada, Eiji; Behl, Christian; Hwang, Shyh‐Lung; Suhardja, L.; Flynn, Gordon L.; Ho, Norman F.H.; Higuchi, William I.

doi:10.1002/jps.2600660221

Cited by 12 publications

(2 citation statements)

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“…The details of the closed vaginal perfusion system have been described before (Owada et al, 1977). Afl:er insertion of the rib cage cell in the vagina of the anesthesized monkey, the vaginal cavity was perfused with normal saline irrigation solution for about 15 min at a flow rate of 20 ml/min to remove exfoliated cells and secretions.…”

Section: Vagina Perfusion Methodsmentioning

confidence: 99%

“…Recently, the methodology in deterrnining vaginal drug absorption in the" female rhesus monkey (Owada et al, 1977) was developed from prototype methods and procedures for studying vaginal absorption in the rabbit doe (Yotsuyanagi et al, 1975). The rabbit lacks a sexual cycle while the rhesus monkey is a sexually cyclical animal closely approximating the human female in many respects.…”

Section: Introductionmentioning

confidence: 99%

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Vaginal drug absorption in the rhesus monkey: Bioavailability method and assessment of estrogens

Park¹,

Langworthy²,

Behl³

et al. 1979

International Journal of Pharmaceutics

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Novel experimental and theoretical methods in evaluating the systemic bioavailability of estrogens delivered via the vaginal route have been developed. The approaches were demonstrated for estrone and estradiol in the rhesus monkey. These newly developed techniques have made it possible to quantify first pass vaginal membrane metabolism for estrone and for estradiol and to disthlguish this process from peripheral tissue metabolism. This was achieved by obtaining steady-state blood levels of the steroids and all significant metabolites resulting from identical zero-order infusion rates of the steroid by the vaginal and intravenous routes. Comparison of the blood levels gave rapid estimations of bioavailability. The modeling of the steady-state situation and quantification of the kinetic parameters were employed such that differences in blood levels from vaginal and intraven~aus drug infusion mirrored the membrane transport and metabolic events. Membrane metabolism of infused estrone and estradiol reduced the blood levels of these steroids by al~out 55 and 61%, respectively, of that expected in the absence of membrane metabolism. About 45% of vaginally administered estrone appeared directly in the blood, as estrone and 9% as estradiol and 46% as total conjugates. The dominant route of membrane metabolism of estrone was estrone conjugation rather than reduction to estiadiol. When estradiol was infused vaginally, 26% estradiol appeared in the blood and 35% as estrone and 39% as total conjugates; the dominant route of metabolism was the ,~xidation to estrone and not estradiol conjugation. * Manuscripts in preparation on vaginal absorption in rhesus monkey of n-alkanols, n-alkanoic acids, estrogens, progesterone and inplanted steroid-silicone rubber vaginal devices.

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Section: Vagina Perfusion Methodsmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%