黏液黏附颊贴的研究进展

Aspee Singh, Upendra Prajapati
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引用次数: 5

摘要

http://dx.doi.org/10.21276/IJRDPL.227 8-0238.2017.6(4)。摘要:口腔是一个极具吸引力的药物输送部位。通过这一途径可以实现粘膜(局部作用)和经粘膜(全身作用)给药。在第一种情况下,目的是实现药物在粘膜上的部位特异性释放,而第二种情况涉及药物通过粘膜屏障吸收到达体循环。通过口腔黏膜的吸收克服了由于胃肠道酶活性和pH值导致的药物过早降解,避免了由于全身前代谢导致的药物活性损失,可以快速实现药物的酸水解和治疗性血浆浓度。这种药物传递平台的粘附特性可以减少酶降解,因为传递载体和吸收膜之间的亲密度增加。然而,口服药物有其缺点,如肝脏首过代谢和胃肠道内酶降解,这就禁止口服某些类型的药物,特别是多肽和蛋白质。因此,其他吸收性粘膜被认为是给药的潜在部位。经黏膜给药途径比口服给药具有明显的优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A review on Mucoadhesive Buccal Patches
http://dx.doi.org/10.21276/IJRDPL.227 8-0238.2017.6(4).2654-2660 ABSTRACT: The oral cavity is an attractive site for the delivery of drugs. Through this route it is possible to realize mucosal (local effect) and transmucosal (systemic effect) drug administration. In the first case, the aim is to achieve a site-specific release of the drug on the mucosa, whereas the second case involves drug absorption through the mucosal barrier to reach the systemic circulation.Absorption through the buccal mucosa overcomes premature drug degradation due to the enzyme activity and pH of gastro intestinal tract, avoids active drug loss due to presystemic metabolism, acid hydrolysis and therapeutic plasma concentration of the drug can be rapidly achieved. The adhesive properties of such drug delivery platforms can reduce the enzymatic degradation due to the increased intimacy between the delivery vehicle and the absorbing membrane. However, per oral administration of drugs has disadvantages such as hepatic first pass metabolism and enzymatic degradation within the GI tract, that prohibit oral administration of certain classes of drugs especially peptides and proteins. Consequently, other absorptive mucosa is considered as potential sites for drug administration. Transmucosal routes of drug delivery offer distinct advantages over per oral administration for systemic drug delivery.
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