Sagar Institute of Research & Technology-Pharmacy, SIRT- Campus Bhopal, India.
J Pharm Pharm Sci. 2010;13(4):571-88. doi: 10.18433/j38w25.
Conventional drug delivery systems have slight control over their drug release and almost no control over the effective concentration at the target site. This kind of dosing pattern may result in constantly changing, unpredictable plasma concentrations. Drugs can be delivered in a controlled pattern over a long period of time by the controlled or modified release drug delivery systems. They include dosage forms for oral and transdermal administration as well as injectable and implantable systems. For most of drugs, oral route remains as the most acceptable route of administration. Certain molecules may have low oral bioavailability because of solubility or permeability limitations. Development of an extended release dosage form also requires reasonable absorption throughout the gastro-intestinal tract (GIT). Among the available techniques to improve the bioavailability of these drugs fabrication of osmotic drug delivery system is the most appropriate one. Osmotic drug delivery systems release the drug with the zero order kinetics which does not depend on the initial concentration and the physiological factors of GIT. This review brings out new technologies, fabrication and recent clinical research in osmotic drug delivery.
传统的药物输送系统对药物释放的控制程度较低,几乎无法控制靶部位的有效浓度。这种给药模式可能导致血浆浓度不断变化,难以预测。通过控制或改良释放药物输送系统,可以长时间以控制的方式输送药物。它们包括口服和透皮给药的剂型以及可注射和可植入系统。对于大多数药物来说,口服途径仍然是最可接受的给药途径。某些分子由于溶解度或通透性限制,口服生物利用度可能较低。延长释放剂型的开发还需要在整个胃肠道(GIT)中具有合理的吸收。在提高这些药物生物利用度的现有技术中,制造渗透药物输送系统是最合适的一种。渗透药物输送系统以零级动力学释放药物,这与初始浓度和 GIT 的生理因素无关。本篇综述介绍了渗透药物输送系统的新技术、制剂和最近的临床研究。