Gupta Sonal, Gabrani Reema, Ali Javed, Dang Shweta
Jaypee Institute of Information Technology, A-10, Sector 62, NOIDA, India.
Recent Pat Drug Deliv Formul. 2011 May;5(2):82-94. doi: 10.2174/187221111795471418.
Vaginal route serves as a potential site of drug administration for local and systemic absorption of a variety of therapeutic agents. Despite being a non- invasive route of drug administration, the vagina has not been extensively explored as compared to other routes. Intravaginal drug delivery has been traditionally restricted to delivery of antinfectives to the local vaginal cavity. Concerted efforts have been made in the recent past to rediscover the vaginal route as a potential route for the delivery of therapeutically important molecules, proteins, peptides, small interfering RNAs, oligonucleotides, antigens, vaccines and hormones. The understanding of vaginal physiology has led to the design of specific intravaginal drug delivery systems to reach the systemic circulation. To overcome the limitations of conventional dosage forms administered through vaginal route various novel approaches like the use of mucoadhesive or bioadhesive polymers, pH- or temperature-sensitive polymers, liposomes, nanoemulsions, nanoparticles, vaginal inserts, multiple emulsions and hydrogels have been designed which enable controlled and prolonged release of drugs. The present article is a comprehensive review of the research and patents encompassing conventional dosage forms used for vaginal drug delivery with emphasis on newer platform technologies pertaining to intravaginal administration.
阴道途径可作为多种治疗药物进行局部和全身吸收给药的潜在部位。尽管它是一种非侵入性给药途径,但与其他途径相比,阴道尚未得到广泛研究。传统上,阴道内给药仅限于将抗感染药物递送至阴道局部腔隙。最近,人们共同努力重新发现阴道途径作为递送具有重要治疗意义的分子、蛋白质、肽、小干扰RNA、寡核苷酸、抗原、疫苗和激素的潜在途径。对阴道生理学的了解促使人们设计出特定的阴道内给药系统以进入体循环。为克服通过阴道途径给药的传统剂型的局限性,人们设计了各种新颖的方法,如使用粘膜粘附或生物粘附聚合物、pH或温度敏感聚合物、脂质体、纳米乳剂、纳米颗粒、阴道插入剂、多重乳剂和水凝胶,这些方法能够实现药物的控释和长效释放。本文是一篇全面综述,涵盖用于阴道给药的传统剂型的研究和专利,重点关注与阴道内给药相关的新型平台技术。