Oxidation-Responsive Polymer-Drug Conjugates with a Phenylboronic Ester Linker

2015 ◽  
Vol 36 (22) ◽  
pp. 2012-2018 ◽  
Author(s):  
Fang-Yi Qiu ◽  
Mei Zhang ◽  
Ran Ji ◽  
Fu-Sheng Du ◽  
Zi-Chen Li
Keyword(s):  
Drug Conjugates ◽  
Responsive Polymer ◽  
Polymer Drug Conjugates

Redox-Responsive Polymer–Drug Conjugates Based on Doxorubicin and Chitosan Oligosaccharide-g-stearic Acid for Cancer Therapy

2015 ◽  
Vol 12 (4) ◽  
pp. 1193-1202 ◽  
Author(s):  
Yigang Su ◽  
Yingwen Hu ◽  
Yongzhong Du ◽  
Xuan Huang ◽  
Jiabei He ◽  
...  
Keyword(s):  
Cancer Therapy ◽  
Stearic Acid ◽  
Chitosan Oligosaccharide ◽  
Drug Conjugates ◽  
Redox Responsive ◽  
Responsive Polymer ◽  
Polymer Drug Conjugates

pH-responsive polymer–drug conjugates as multifunctional micelles for cancer-drug delivery

2014 ◽  
Vol 25 (33) ◽  
pp. 335101 ◽  
Author(s):  
Yang Kang ◽  
Wei Ha ◽  
Ying-Qian Liu ◽  
Yuan Ma ◽  
Min-Min Fan ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Cancer Drug ◽  
Ph Responsive ◽  
Drug Conjugates ◽  
Responsive Polymer ◽  
Cancer Drug Delivery ◽  
Polymer Drug Conjugates

pH-responsive polymer–drug conjugates: Design and progress

2016 ◽  
Vol 222 ◽  
pp. 116-129 ◽  
Author(s):  
Xin Pang ◽  
Yue Jiang ◽  
Qicai Xiao ◽  
Albert Wingnang Leung ◽  
Heyu Hua ◽  
...  
Keyword(s):  
Ph Responsive ◽  
Drug Conjugates ◽  
Responsive Polymer ◽  
Polymer Drug Conjugates

Design, Synthesis and Studies on Novel Polymeric Prodrugs of Erlotinib for Colon Drug Delivery

2020 ◽  
Vol 20 ◽  
Author(s):  
Sahil Kumar ◽  
Bandna Sharma ◽  
Tilak R. Bhardwaj ◽  
Rajesh K. Singh
Keyword(s):  
Drug Delivery ◽  
Colon Cancer ◽  
Drug Release ◽  
Anticancer Agents ◽  
Release Kinetics ◽  
In Vitro Release ◽  
Specific Treatment ◽  
Drug Conjugates ◽  
Polymer Drug Conjugates

Aims: In the present study, polymer-drug conjugates were synthesized based on azo-bond cleavage drug delivery approach for targeting erlotinib as anticancer drug specifically to the colon for the proficient treatment of colon cancer. Background: Colon cancer (CC) is the third commonly detected tumor worldwide and it make up about 10 % of all cases of cancers. Most of the chemotherapeutic drugs available for treating colon cancer are not only toxic to cancerous cells but also to the normal healthy cells. Among the various approaches to get rid of the adverse effects of anticancer agents, prodrugs are one of the most imperative approaches. Objective: The objective of the study is to chemically modify the erlotinib drug through azo-bond linkage and suitable spacer which will be finally linked to polymeric backbone to give desired polymer linked prodrug. The azo reductase enzyme present in colon is supposed to cleave the azo-bond specifically and augment the drug release at the colon. Methods: The synthesized conjugates were characterized by IR and 1H-NMR spectroscopy. The cleavage of aromatic azobond resulted in a potential colon-specific liberation of drug from conjugate studied in rat fecal contents. In vitro release profiles of polyphosphazene-linked conjugates of erlotinib have been studied at pH 1.2, pH 6.8 and pH 7.4. The stability study was designed to exhibit that free drug was released proficiently and unmodified from polyphosphazene-erlotinib conjugates having aromatic azo-bond in artificial colon conditions. Results: The synthesized conjugates were demonstrated to be stable in simulated upper gastro-intestinal tract conditions. The drug release kinetics shows that all the polymer-drug conjugates of erlotinib follow zero-order release kinetics which indicates that the drug release from the polymeric backbone is independent of its concentration. Kinetic study of conjugates with slope (n) shows the anomalous type of release with an exponent (n) > 0.89 indicating a super case II type of release. Conclusion: These studies indicate that polyphosphazene linked drug conjugates of erlotinib could be the promising candidates for the site-specific treatment of colon cancer with least detrimental side-effects.

scholarly journals Folic Acid-Targeted Paclitaxel-Polymer Conjugates Exert Selective Cytotoxicity and Modulate Invasiveness of Colon Cancer Cells

Pharmaceutics ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 929
Author(s):  
Antonella Grigoletto ◽  
Gabriele Martinez ◽  
Daniela Gabbia ◽  
Tommaso Tedeschini ◽  
Michela Scaffidi ◽  
...  
Keyword(s):  
Folic Acid ◽  
Cancer Cells ◽  
Pharmacokinetic Profile ◽  
Strong Impact ◽  
Passive Targeting ◽  
Drug Conjugates ◽  
Tumor Delivery ◽  
The Right ◽  
Polymer Drug Conjugates ◽  
Ht 29

Although selective tumor delivery of anticancer drugs has been sought by exploiting either passive targeting or by ligand-mediated targeting, a selective anticancer therapy remains an unmet medical need. Despite the advances which have been achieved by nanomedicines, nanosystems such as polymer-drug conjugates still miss the goal of clinical efficacy. In this study, we demonstrated that polymer-drug conjugates require a thoroughly chemical design and the right targeting agent/polymer ratio to be selective and effective towards cancer cells. In particular, two PEG conjugates carrying paclitaxel and targeted with different folic acid (FA)/PEG ratios (one or three) were investigated. The cytotoxicity study in positive (HT-29) and negative (HCT-15) FA receptor (FR)-cell lines demonstrated that the conjugates with one or three FAs were 4- or 28-fold more active in HT-29 cells, respectively. The higher activity of the 3-FA conjugate was confirmed by its strong impact on cell cycle arrest. Furthermore, FA targeting had a clear effect on migration and invasiveness of HT-29 cells, which were significantly reduced by both conjugates. Interestingly, the 3-FA conjugate showed also an improved pharmacokinetic profile in mice. The results of this study indicate that thorough investigations are needed to optimize and tune drug delivery and achieve the desired selectivity and activity towards cancer cells.

Long-Circulating and Passively Tumor-Targeted Polymer-Drug Conjugates Improve the Efficacy and Reduce the Toxicity of Radiochemotherapy

2010 ◽  
Vol 12 (9) ◽  
pp. B413-B421 ◽  
Author(s):  
Twan Lammers ◽  
Vladimir Subr ◽  
Karel Ulbrich ◽  
Peter Peschke ◽  
Peter E. Huber ◽  
...  
Keyword(s):  
Drug Conjugates ◽  
Polymer Drug Conjugates
Sign in / Sign up

Export Citation Format

Share Document