PEG-SS-PPS:  Reduction-Sensitive Disulfide Block Copolymer Vesicles for Intracellular Drug Delivery

2007 ◽  
Vol 8 (6) ◽  
pp. 1966-1972 ◽  
Author(s):  
Simona Cerritelli ◽  
Diana Velluto ◽  
Jeffrey A. Hubbell
Keyword(s):  
Drug Delivery ◽  
Block Copolymer ◽  
Intracellular Drug Delivery

Tumor-targeting intracellular drug delivery based on dual acid/reduction-degradable nanoassemblies with ketal interface and disulfide core locations

2019 ◽  
Vol 10 (22) ◽  
pp. 2840-2853 ◽  
Author(s):  
Arman Moini Jazani ◽  
Newsha Arezi ◽  
Chaitra Shetty ◽  
Sung Hwa Hong ◽  
Haowen Li ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Block Copolymer ◽  
Drug Release ◽  
Tumor Targeting ◽  
Intracellular Drug Delivery ◽  
Acid Reduction

Dual acid/reduction-degradable block copolymer nanoassemblies both at core/corona interfaces and in micellar cores leading to synergistic and accelerated drug release for robust tumor-targeting intracellular drug delivery.

Shell-Detachable Micelles Based on Disulfide-Linked Block Copolymer As Potential Carrier for Intracellular Drug Delivery

2009 ◽  
Vol 20 (6) ◽  
pp. 1095-1099 ◽  
Author(s):  
Ling-Yan Tang ◽  
Yu-Cai Wang ◽  
Yang Li ◽  
Jin-Zhi Du ◽  
Jun Wang
Keyword(s):  
Drug Delivery ◽  
Block Copolymer ◽  
Intracellular Drug Delivery

K+ -Responsive Block Copolymer Micelles for Targeted Intracellular Drug Delivery

2017 ◽  
Vol 17 (9) ◽  
pp. 1700143 ◽  
Author(s):  
Shan Yan ◽  
Lin-Yan Wan ◽  
Xiao-Jie Ju ◽  
Jiang-Feng Wu ◽  
Lei Zhang ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Block Copolymer ◽  
Intracellular Drug Delivery ◽  
Block Copolymer Micelles ◽  
Copolymer Micelles

Imidazole‐Mediated Dual Location Disassembly of Acid‐Degradable Intracellular Drug Delivery Block Copolymer Nanoassemblies

2021 ◽  
pp. 2100262
Author(s):  
Arman Moini Jazani ◽  
Chaitra Shetty ◽  
Hourieh Movasat ◽  
Kamaljeet Kaur Bawa ◽  
Jung Kwon Oh
Keyword(s):  
Drug Delivery ◽  
Block Copolymer ◽  
Intracellular Drug Delivery

Synthesis and micellization of block copolymer based on host–guest recognition and double disulphide linkage for intracellular drug delivery

2017 ◽  
Vol 75 (3) ◽  
pp. 1149-1169 ◽  
Author(s):  
Zhen Zhang ◽  
Changyu He ◽  
Lianjiang Tan ◽  
Bingya Liu ◽  
Zhenggang Zhu ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Block Copolymer ◽  
Intracellular Drug Delivery

Rosin-based block copolymer intracellular delivery nanocarriers with reduction-responsive sheddable coronas for cancer therapy

2016 ◽  
Vol 7 (29) ◽  
pp. 4751-4760 ◽  
Author(s):  
So Young An ◽  
Sung Hwa Hong ◽  
Chuanbing Tang ◽  
Jung Kwon Oh
Keyword(s):  
Drug Delivery ◽  
Block Copolymer ◽  
Cancer Therapy ◽  
Anticancer Drugs ◽  
Colloidal Stability ◽  
Intracellular Delivery ◽  
Intracellular Drug Delivery

Rosin-based, reduction-responsive block copolymer-based nanocarriers exhibiting excellent colloidal stability enabling the delivery of anticancer drugs to cancerous tissues for the enhanced release of encapsulated drugs, offering great versatility as intracellular drug-delivery nanocarriers for cancer therapy.

Chitosan oligosaccharide copolymer micelles with double disulphide linkage in the backbone associated by H-bonding duplexes for targeted intracellular drug delivery

2015 ◽  
Vol 6 (9) ◽  
pp. 1454-1464 ◽  
Author(s):  
Qinglai Yang ◽  
Changyu He ◽  
Yuhong Xu ◽  
Bingya Liu ◽  
Zhifeng Shao ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Folic Acid ◽  
Block Copolymer ◽  
Chitosan Oligosaccharide ◽  
Intracellular Drug Delivery ◽  
Block Copolymer Micelles ◽  
Copolymer Micelles

Folic acid conjugated block copolymer micelles with H-bonding associated double disulphide linkage in the backbone were developed.

Disassembly and tumor-targeting drug delivery of reduction-responsive degradable block copolymer nanoassemblies

2019 ◽  
Vol 10 (13) ◽  
pp. 1554-1568 ◽  
Author(s):  
Jung Kwon Oh
Keyword(s):  
Drug Delivery ◽  
Block Copolymer ◽  
Block Copolymers ◽  
Tumor Targeting ◽  
Intracellular Drug Delivery ◽  
Disulfide Linkages

Review on recent strategies to synthesize novel disulfide-containing reductively-degradable block copolymers and their nanoassemblies as being classified with the number, position, and location of the disulfide linkages toward effective tumor-targeting intracellular drug delivery exhibiting enhanced release of encapsulated drugs.

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