Development polymeric micellar system for targeted delivery of antitumor drugs

Author(s):  
L. Kunitskaya ◽  
T. Zheltonozhskaya ◽  
V. Gerda ◽  
V. Klepko
2014 ◽  
Vol 16 (3) ◽  
pp. 600-608 ◽  
Author(s):  
Yichao Chen ◽  
Xiaolan Zhang ◽  
Jianqin Lu ◽  
Yixian Huang ◽  
Jiang Li ◽  
...  

2018 ◽  
Vol 14 (8) ◽  
pp. 1420-1429 ◽  
Author(s):  
Mimi Lin ◽  
Suyan Shan ◽  
Peipei Liu ◽  
Liwei Ma ◽  
Libin Huang ◽  
...  

2021 ◽  
Vol 28 ◽  
Author(s):  
Xi Wang ◽  
Yiming Chen ◽  
Yongjuan Wang ◽  
Bangmao Wang ◽  
Jie Zhang ◽  
...  

: PEPT1 is a vital member of the proton-dependent oligopeptide transporters family (POTs). Many studies have confirmed that PEPT1 plays a critical role in the absorption of dipeptides, tripeptides, and pseudopeptides in the intestinal tract. In recent years, several studies have found that PEPT1 is highly expressed in malignant tumor tissues and cells. The abnormal expression of PEPT1 in tumors may be closely related to the progress of tumors, and hence, could be considered as a potential molecular biomarker for the diagnosis, treatment, and prognosis in malignant tumors. Furthermore, PEPT1 can be used as the delivery target to mediate the targeted delivery of antitumor drugs. Herein, the expression, regulation, and role of PEPT1 in tumors in recent years were reviewed.


Author(s):  
Juan Liu ◽  
Xixue Hu ◽  
Shubin Jin ◽  
Xing-Jie Liang ◽  
Xiaowei Ma

Rapid release and clearance of antitumor drugs in vivo are the main factors to evade the effectiveness of chemotherapeutics. Targeted delivery and controlled release of drugs are the most pressing...


2019 ◽  
Vol 43 (44) ◽  
pp. 17284-17297 ◽  
Author(s):  
Fangxiang Song ◽  
Yan Li ◽  
Shuai Wang ◽  
Li Zhang ◽  
QianLin Chen

Herein, dual-mesoporous structure silica (with pore sizes from 2 to 4 nm and from 4 to 16 nm) simultaneously modified with amino and carboxyl groups was successfully synthesized.


2011 ◽  
Vol 21 (25) ◽  
pp. 9185 ◽  
Author(s):  
Sasmita Mohapatra ◽  
Smruti R. Rout ◽  
Swatilekha Maiti ◽  
Tapas K. Maiti ◽  
Asit B. Panda

2019 ◽  
Vol 24 (43) ◽  
pp. 5207-5218 ◽  
Author(s):  
H.V. Grushevskaya ◽  
N.G. Krylova

<P>Background: In spite of considerable efforts of researchers the cancer deseases remain to be incurable and a percentage of cancer deseases in the structure of mortality increases every year. At that, high systemic toxicity of antitumor drugs hampers their effective use. Because of this fact, the development of nanosystems for targeted delivery of antitumor drugs is one of the leading problem in nanomedicine and nanopharmacy. </P><P> Objective: To critically examine the modern strategies for carbon nanotubes (CNTs)-based delivery of anticancer quinones and to summarize the mechanisms which can provide high effectiveness and multifunctionality of the CNT-based quinone delivery platform. </P><P> Results: Quinones, including anthracycline antibiotics – doxorubicin and daunorubicin, are among the most prospective group of natural and syntetic compounds which exhibit high antitumor activity against different type of tumors. In this review, we focus on the possibilities of using CNTs for targeted delivery of antitumor compounds with quinoid moiety which is ordinarily characterized by high specific interaction with DNA molecules. Quinones can be non-covalently adsorbed on CNT surface due to their aromatic structure and π-conjugated system of double bonds. The characteristic features of doxorubicine-CNT complex are high loading efficiency, pH-dependent release in acidic tumor microenviroment, enough stability in biological fluid. Different types of CNT functionalization, targeting strategies and designs for multifunctional CNT-based doxorubicine delivery platform are disscussed. </P><P> Conclusion: Nanosystems based on functionalized CNTs are very promising platform for quinone delivery resulting in significant enhancement of cancer treatment efficiency. Functionalization of CNTs with the polymeric shell, especially DNA-based shells, can provide the greatest affinity and mimicry with biological structures.</P>


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