Priyanka R Kulkarni, Jaydeep D Yadav, K. A. Vaidya, D. M. V. P. Samaj 's
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引用次数: 14
摘要
几乎从发现脂质体囊泡并证明其夹持潜力开始,脂质体囊泡就作为可用于治疗的各种生物活性分子的潜在载体引起了研究人员的关注。自 1970 年以来,人们一直在广泛研究脂质体作为药物载体如何将治疗药物更好地输送到体内特定部位。脂质体是一种可生物降解且基本无毒的载体,可以包裹亲水性和疏水性材料,在给药系统中被用作药物载体。因此,这项技术已经得到了许多改进,从而有可能在临床上用于治疗某些疾病。许多以脂质体为基础的 DNA 给药系统已被描述,其中包括用于靶向特定细胞表面受体或从溶酶体区逃逸的分子成分。从脂质体给药系统的临床应用中获得的洞察力现在可以整合到脂质体的设计中,无论脂质体膜上是否表达目标识别分子,脂质体都可以靶向组织、细胞或细胞内分区。脂质体作为药物载体所取得的成功体现在许多基于脂质体的制剂上,这些制剂已在市场上销售或正在进行临床试验。
Almost from the time of their discovery the demonstration of their entrapment potential, liposomal vesicles have drawn attention of researchers as potential carriers of various bioactive molecules that could be used for therapeutic applications. Liposomes have been widely investigated since 1970 as drug carriers for improving the delivery of therapeutic agents to specific sites in the body. Liposomes, which are biodegradable and essentially non‐toxic vehicles, can encapsulate both hydrophilic and hydrophobic materials, and are utilized as drug carriers in drug delivery systems. As a result, numerous improvements have been made, thus making this technology potentially useful for the treatment of certain diseases in the clinics. Many liposome‐based DNA delivery systems have been described, including molecular components for targeting given cell surface receptors or for escaping from the lysosomal compartment. The insight gained from clinical use of liposome drug delivery systems can now be integrated to design liposomes that can be targeted on tissues, cells or intracellular compartments with or without expression of target recognition molecules on liposome membranes. The success of liposomes as drug carriers has been reflected in a number of liposome‐based formulations, which are commercially available or are currently undergoing clinical trials.