Amphiphilic photocleavable block copolymers based on monomethyl poly(ethylene glycol) and poly(4-substituted-ε-caprolactone): synthesis, characterization, and cellular uptake
This paper presents the synthesis of a novel amphiphilic block copolymer containing photodegradable linkers as junction points between hydrophilic and hydrophobic chains. MPEG-ONB-PXCL block copolymers were synthesized by a combination of ROP and "clicks" from a difunctional photoresponsiv...
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Published in | RSC advances Vol. 3; no. 40; pp. 18453 - 18463 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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01.01.2013
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Abstract | This paper presents the synthesis of a novel amphiphilic block copolymer containing photodegradable linkers as junction points between hydrophilic and hydrophobic chains. MPEG-ONB-PXCL block copolymers were synthesized by a combination of ROP and "clicks" from a difunctional photoresponsive initiator (ONB). The copolymers are biodegradable and biocompatible, and can self-assemble into photoresponsive micelles. When polymer solutions were exposed to UV, we observed significant changes in the structure and morphology of particles. Fluorescence emission measurements showed that Nile red (NR), a hydrophobic dye, encapsulated by the MPEG-ONB-PXCL micelles, is released upon irradiation because of disruption of the micelles. Light-triggered bursts were observed for Indomethacin (IMC)-loaded MPEG-ONB-PXCL micelles upon at 30 min of light irradiation. No significant toxicity of these nanoparticles was found, at concentrations up to 1000 mu g mL super(-1), before or after light irradiation. The doxorubicin (DOX)-loaded micelles facilitated improved uptake of DOX by HeLa cells within 60 min, and were retained primarily in the cytoplasm. |
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AbstractList | This paper presents the synthesis of a novel amphiphilic block copolymer containing photodegradable linkers as junction points between hydrophilic and hydrophobic chains. MPEG-ONB-PXCL block copolymers were synthesized by a combination of ROP and “clicks” from a difunctional photoresponsive initiator (ONB). The copolymers are biodegradable and biocompatible, and can self-assemble into photoresponsive micelles. When polymer solutions were exposed to UV, we observed significant changes in the structure and morphology of particles. Fluorescence emission measurements showed that Nile red (NR), a hydrophobic dye, encapsulated by the MPEG-ONB-PXCL micelles, is released upon irradiation because of disruption of the micelles. Light-triggered bursts were observed for Indomethacin (IMC)-loaded MPEG-ONB-PXCL micelles upon at 30 min of light irradiation. No significant toxicity of these nanoparticles was found, at concentrations up to 1000 μg mL⁻¹, before or after light irradiation. The doxorubicin (DOX)-loaded micelles facilitated improved uptake of DOX by HeLa cells within 60 min, and were retained primarily in the cytoplasm. This paper presents the synthesis of a novel amphiphilic block copolymer containing photodegradable linkers as junction points between hydrophilic and hydrophobic chains. MPEG-ONB-PXCL block copolymers were synthesized by a combination of ROP and "clicks" from a difunctional photoresponsive initiator (ONB). The copolymers are biodegradable and biocompatible, and can self-assemble into photoresponsive micelles. When polymer solutions were exposed to UV, we observed significant changes in the structure and morphology of particles. Fluorescence emission measurements showed that Nile red (NR), a hydrophobic dye, encapsulated by the MPEG-ONB-PXCL micelles, is released upon irradiation because of disruption of the micelles. Light-triggered bursts were observed for Indomethacin (IMC)-loaded MPEG-ONB-PXCL micelles upon at 30 min of light irradiation. No significant toxicity of these nanoparticles was found, at concentrations up to 1000 mu g mL super(-1), before or after light irradiation. The doxorubicin (DOX)-loaded micelles facilitated improved uptake of DOX by HeLa cells within 60 min, and were retained primarily in the cytoplasm. |
Author | Lee, Ren-Shen Peng, Kang-Yu Hua, Mu-Yi Wang, Shiu-Wei |
Author_xml | – sequence: 1 givenname: Kang-Yu surname: Peng fullname: Peng, Kang-Yu – sequence: 2 givenname: Shiu-Wei surname: Wang fullname: Wang, Shiu-Wei – sequence: 3 givenname: Mu-Yi surname: Hua fullname: Hua, Mu-Yi – sequence: 4 givenname: Ren-Shen surname: Lee fullname: Lee, Ren-Shen |
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CitedBy_id | crossref_primary_10_1039_C4PY01628A crossref_primary_10_1080_00914037_2018_1539987 crossref_primary_10_1016_j_reactfunctpolym_2015_08_009 crossref_primary_10_1016_j_carbpol_2014_09_062 crossref_primary_10_1080_10601325_2020_1814158 crossref_primary_10_3389_fphar_2024_1356639 crossref_primary_10_1039_C4RA03043E crossref_primary_10_1007_s10965_015_0803_6 crossref_primary_10_1039_C6PY01455K |
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SubjectTerms | Biocompatibility biodegradability Block copolymers Cellular composite polymers cytoplasm doxorubicin dyes encapsulation fluorescence hydrophilicity hydrophobicity indomethacin irradiation lactones Light irradiation Micelles nanoparticles polyethylene glycol Synthesis Toxicity Uptakes |
Title | Amphiphilic photocleavable block copolymers based on monomethyl poly(ethylene glycol) and poly(4-substituted-ε-caprolactone): synthesis, characterization, and cellular uptake |
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