Exploring the Therapeutic Potential of Anticancer Heterocyclic Compounds: Role in Nanoscale Pharmacotherapy

被引:0
|
作者
Kumar, Lalit [1 ,2 ]
Verma, Shivani [3 ]
Joshi, Kajal [4 ]
Sharma, Sumit [5 ]
机构
[1] Himachal Inst Pharmaceut Educ & Res, Dept Pharmaceut, Nadaun 177033, Himachal Prades, India
[2] Sri Sai Coll Pharm, Dept Pharmaceut, Manawala 143149, Punjab, India
[3] Govt Punjab, Dept Hlth & Family Welf, Chandigarh 160022, India
[4] Himachal Inst Pharmaceut Educ & Res, Dept Pharmacol, Nadaun 177033, Himachal Prades, India
[5] Delhi Pharmaceut Sci & Res Univ, New Delhi 110017, India
关键词
anticancer; heterocyclic; intrinsic; nanocarriers; pharmacokinetic; pharmacodynamic; LIPOSOMAL DAUNORUBICIN DAUNOXOME; STABILIZED GOLD NANOPARTICLES; DRUG-DELIVERY; BIOLOGICAL EVALUATION; POLYMERIC MICELLES; TARGETED DELIVERY; IN-VITRO; HYBRID NANOPARTICLES; VINCRISTINE SULFATE; CANCER-THERAPY;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
There are a large number of pharmaceutical products in the market containing heterocyclic compounds. Heterocyclic compounds are explored in the field of therapeutics due to their unique physicochemical and pharmacological properties. A large number of heterocyclic compounds existing in the pharmaceutical market have marked anticancer activity and many of them are under research investigations to treat different types of cancers. Anticancer heterocyclic compounds show many shortcomings such as other anticancer agents in bioavailability and site -specific drug delivery resulting in toxicity and decreased patient compliance. These shortcomings can be eliminated by applying the principles of nanotechnology. The present review discloses the biochemical mechanism of action, different biological targets, intrinsic shortcomings, and structure-activity relationships of anticancer heterocyclic compounds. Furthermore, the role of different nanocarrier systems in selective biological targeting and alteration of pharmacokinetic and pharmacodynamic characteristics of anticancer heterocyclic compounds will be discussed in detail.
引用
收藏
页码:47 / 94
页数:48
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