Li C, Bhatt P P, Johnston T P
Division of Pharmaceutics and Pharmacodynamics, College of Pharmacy, University of Illinois at Chicago 60612, USA.
Pharm Dev Technol. 1997 Aug;2(3):265-74. doi: 10.3109/10837459709031446.
A biocompatible, mucoadhesive buccal patch was evaluated in rabbits for transmucosal delivery of peptides. Oxytocin (OT) was incorporated into custom coformulations of Carbopol 974P and silicone polymer and the resulting plasma OT concentration versus time profiles determined following patch application. For comparative purposes, the mean values determined for the elimination half-life (t1/2), volume of distribution (Vd), and the total body clearance (CL) following intravenous injection of OT were 2.9 +/- 0.2 min, 85.3 +/- 6.7 ml, and 20.4 +/- 2.03 ml/min, respectively. Following application of oxytocin-loaded mucoadhesive patches, plasma OT concentrations remained 20- to 28-fold greater from 0.5 to 3.0 hr than control animals administered placebo patches. The steady-state plasma OT concentration (Css) following application of the buccal patches was 80.6 +/- 15.9 pg/ml. The lag-time associated with attainment of the Css was 0.45 +/- 0.18 hr. Steady-state flux (Jss) of oxytocin in vivo was 139 +/- 36.8 ng/hr/cm2. Based on the amount of OT remaining in the patches following removal, the average dose of OT released in vivo was 0.27 +/- 0.024 mg with a bioavailability of 0.1%. No significant alterations in mucosal histology were observed when underlying mucosa to which OT patches had been applied were compared to either control (no patch) mucosa or mucosa underneath placebo patches. The mucoadhesive buccal patches were easy to apply and remove, nonirritating to tissue, and able to continuously deliver a nonapeptide over 3 hr. Based on these preliminary studies, the mucoadhesive buccal patches evaluated may represent an improved transmucosal drug delivery system for peptides and conventional drug substances.
在兔体内对一种生物相容性、粘膜粘附性口腔贴片进行了评估,用于肽的经粘膜递送。将催产素(OT)加入到卡波姆974P和硅酮聚合物的定制共混物中,并在贴片应用后测定所得血浆OT浓度随时间的变化曲线。为作比较,静脉注射OT后测定的消除半衰期(t1/2)、分布容积(Vd)和全身清除率(CL)的平均值分别为2.9±0.2分钟、85.3±6.7毫升和20.4±2.03毫升/分钟。应用载有催产素的粘膜粘附贴片后,在0.5至3.0小时内,血浆OT浓度比给予安慰剂贴片的对照动物高20至28倍。应用口腔贴片后的稳态血浆OT浓度(Css)为80.6±15.9皮克/毫升。达到Css的滞后时间为0.45±0.18小时。催产素在体内的稳态通量(Jss)为139±36.8纳克/小时/平方厘米。根据移除后贴片中剩余的OT量,OT在体内释放的平均剂量为0.27±0.024毫克,生物利用度为0.1%。将应用OT贴片后的下层粘膜与对照(未贴片)粘膜或安慰剂贴片下的粘膜进行比较时,未观察到粘膜组织学有明显改变。粘膜粘附性口腔贴片易于应用和移除,对组织无刺激性,并且能够在3小时内持续递送九肽。基于这些初步研究,所评估的粘膜粘附性口腔贴片可能代表了一种用于肽和传统药物的改进的经粘膜给药系统。