摘要
有效的药物投递系统对于新药开发是极其重要的。以遵循医学的个体化医疗(EBMP)能够在正确的时间投递精确的药物到合适的患者身上,其涵盖了临床意义上的基因倾向和纳米配方的时辰药理学方面。最近纳米技术在细胞、分子和基因水平提供了临床显著信息来促进遵循医学以证据为基础的个体化治疗。尤其是用聚乙二醇封装的脂质体药物已经提高了癌症、心血管疾病、神经退行性疾病的药效学。长循环脂质体和成块共聚物在实体瘤中通过增强渗透率和保留(EPR)作用而缓慢聚集,对癌症化疗中药物投递具有重要意义。小分子干扰核糖核苷酸siRNA和寡核苷酸对抑制潜在耐受多种药物(MDR)的恶性肿瘤细胞的选择靶向性上也已经显示出了潜力。另外,植入式药物投递装置已经提高了一些慢性疾病的治疗。近年来,微RNA、金属硫蛋白(MTs)、α-突触核蛋白指数和Charnoly体(CB)已成为几种药物开发生物标记物作为新药发现生物标记物出现。CB拮抗剂-负荷ROS靶向清除的纳米颗粒(NPs)可能在神经退行性疾病和心脑血管疾病的治疗中有所发展。CBs 在过增生性细胞中的非特异性诱导可能引起脱发、胃肠道(GIT)症状、骨髓抑制、神经毒性和不孕。因此选择性CB受体激动剂可能会发展成增加癌症干细胞特异性CB生成以根除MDR恶性肿瘤,并且很少或没有毒副作用。本文重点阐述了采用新兴的纳米疗法实现EBPM安全、经济和有效治疗神经退行性疾病、心血管疾病和癌症中的新进展。
关键词: Charnloy体,charnolophagy
Current Drug Targets
Title:Nanotheranostics in Evidence Based Personalized Medicine
Volume: 15 Issue: 10
Author(s): Sushil Sharma
Affiliation:
关键词: Charnloy体,charnolophagy
摘要: Efficient drug delivery systems are exceedingly important for novel drug discovery. The evidence-based personalized medicine (EBPM) promises to deliver the right drug at the right time to a right patient as it covers clinicallysignificant genetic predisposition and chronopharmacological aspects of nanotheranostics. Recently nanotechnology has provided clinically-significant information at the cellular, molecular, and genetic level to facilitate evidence-based personalized treatment. Particularly drug encapsulation in pegylated liposomes has improved pharmacodynamics of cancer, cardiovascular diseases, and neurodegenerative diseases. Long-circulating liposomes and block copolymers concentrate slowly via enhanced permeability and retention (EPR) effect in the solid tumors and are highly significant for the drug delivery in cancer chemotherapeutics. Selective targeting of siRNA and oligonucleotides to tumor cells with a potential to inhibit multi-drug resistant (MDR) malignancies has also shown promise. In addition, implantable drug delivery devices have improved the treatment of several chronic diseases. Recently, microRNA, metallothioneins (MTs), α-synuclein index, and Charnoly body (CB) have emerged as novel drug discovery biomarkers. Hence CB antagonists-loaded ROSscavenging targeted nanoparticles (NPs) may be developed for the treatment of neurodegenerative and cardiovascular diseases. Nonspecific induction of CBs in the hyper-proliferative cells may cause alopecia, gastrointestinal tract (GIT) symptoms, myelosuppression, neurotoxicity, and infertility. Therefore selective CB agonists may be developed to augment cancer stem cell specific CB formation to eradicate MDR malignancies with minimum or no adverse effects. This review highlights recent advances on safe, economical, and effective treatment of neurodegenerative diseases, cardiovascular diseases, and cancer by adopting emerging nanotheranostic strategies to accomplish EBPM.
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Cite this article as:
Sharma Sushil, Nanotheranostics in Evidence Based Personalized Medicine, Current Drug Targets 2014; 15 (10) . https://dx.doi.org/10.2174/1389450115666140826123552
DOI https://dx.doi.org/10.2174/1389450115666140826123552 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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