Hussain M A, Aungst B J, Kapil R, Mousa S A
DuPont Merck Pharmaceutical Company, Wilmington, DE 19880-0400, USA.
J Pharm Sci. 1997 Dec;86(12):1358-60. doi: 10.1021/js970208r.
Intranasal absorption and bioavailability of DMP 755, a peptidomimetic, platelet glycoprotein IIb/IIIa receptor antagonist, were examined in anesthetized and lightly sedated dogs. Nasal bioavailability was determined by measuring plasma concentrations relative to those after intravenous dosing. DMP 755 is an ester prodrug, and bioavailability reflects concentrations of the acid hydrolysis product. Nasal bioavailability in dogs anesthetized with pentobarbital was 85 +/- 4%, whereas in dogs anesthetized with the short-acting anesthetic propofol, bioavailability was 32 +/- 7%. Nasal bioavailability was greater than the reported oral bioavailability of DMP 755 in dogs, and was quite consistent. Because anesthesia affects nasal bioavailability, an effect that may depend on the absorption half-life of the test compound, a conscious or lightly sedated animal model is preferred.
在麻醉和轻度镇静的犬类中研究了拟肽类血小板糖蛋白IIb/IIIa受体拮抗剂DMP 755的鼻腔吸收和生物利用度。通过测量相对于静脉给药后的血浆浓度来确定鼻腔生物利用度。DMP 755是一种酯前药,生物利用度反映了酸水解产物的浓度。用戊巴比妥麻醉的犬类的鼻腔生物利用度为85±4%,而用短效麻醉剂丙泊酚麻醉的犬类的生物利用度为32±7%。鼻腔生物利用度大于报道的犬类中DMP 755的口服生物利用度,且相当一致。由于麻醉会影响鼻腔生物利用度,这种影响可能取决于受试化合物的吸收半衰期,因此优选清醒或轻度镇静的动物模型。