Clinical experience with drug delivery systems as tools to decrease the toxicity of anticancer chemotherapeutic agents

毒性 药理学 药物输送 医学 药品 脂质体 靶向给药 紫杉醇 治疗指标 依托泊苷 毒品携带者 体内 化疗 化学 内科学 生物 生物技术 有机化学 生物化学
作者
Raul C. Maranhão,Carolina Graziani Vital,Thauany Martins Tavoni,Silvia Graziani
出处
期刊:Expert Opinion on Drug Delivery [Taylor & Francis]
卷期号:14 (10): 1217-1226 被引量:45
标识
DOI:10.1080/17425247.2017.1276560
摘要

Introduction: The toxicity of chemotherapeutic agents, resulting from their low pharmacological index, introduces considerable discomfort and risk to cancer patients. Among several strategies to reduce the toxicity of chemotherapeutic agents, targeted drug delivery is the most promising one.Areas covered: Liposomes, micelles, albumin-based, polymeric, dendritic and lipid core nanoparticles have been used as carriers to concentrate anticancer drugs in neoplastic tissues, and clinical studies of those preparations are reviewed. In most clinical studies, drug delivery systems reduced drug toxicity. Lipid core nanoparticles (LDE) that bind to cell lipoprotein receptors have the ability to concentrate in neoplastic tissues and were the first artificial non-liposomal system shown in in vivo studies to possess targeting properties. The toxicity reduction achieved by LDE as vehicle of carmustine, etoposide and paclitaxel was singularly strong.Expert opinion: The reduced toxicity offered by drug delivery systems has expanded treatment population that may benefit from chemotherapy including feeble, overtreated and elderly patients that would otherwise be offered palliative therapy. Drug delivery systems may either prolong the duration of treatments or allow increases in drug dose.
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