Fast and Reversible Photoresponsive Self-Assembly Behavior of Rosin-Based Amphiphilic Polymers

被引:4
作者
Li, Wanbing [1 ,2 ,3 ,4 ,5 ,6 ]
Zhang, Haibo [1 ,2 ,3 ,4 ,5 ,6 ]
Zhai, Zhaolan [1 ,2 ,3 ,4 ,5 ,6 ]
Huang, Xujuan [6 ,7 ]
Shang, Shibin [1 ,2 ,3 ,4 ,5 ,6 ]
Song, Zhanqian [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Natl Forestry & Grassland Adm, Inst Chem Ind Forest Prod, Natl Engn Lab Biomass Chem Utilizat, Key Lab Chem Engn Forest Prod, Nanjing 210042, Jiangsu, Peoples R China
[2] Inst Chem Ind Forest Prod, CAF, Nanjing 210042, Jiangsu, Peoples R China
[3] Natl Engn Lab Biomass Chem Utilizat, Instituteof Chem Ind Forest Prod, Nanjing 210042, Jiangsu, Peoples R China
[4] Natl Forestry & Grassland Adm, Key Lab Chem Engn Forest Prod, Instituteof Chem Ind Forest Prod, Nanjing 210042, Jiangsu, Peoples R China
[5] Inst Chem Ind Forest Prod, Key Lab Biomass Energy & Mat, Nanjing 210042, Jiangsu, Peoples R China
[6] Nanjing Forestry Univ, Coinnovat Ctr Efficient Proc & Utilizat Forest Res, Nanjing 210037, Peoples R China
[7] Yancheng Inst Technol, Sch Chem & Chem, Yancheng 210042, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
rosin; amphiphilic polymers; photo-responsive; self-assembly; morpholog y evolution; VISIBLE-LIGHT; MICELLES; SURFACTANT; COPOLYMERS; PH; DELIVERY; DESIGN; DRUG;
D O I
10.1021/acs.jafc.2c04389
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Designing stimulus-responsive amphiphilic polymers with a fast photoresponsive self-assembly behavior remains a challenge. Two series of rosin-terminated and azobenzene-terminated amphiphilic polymers (PAMn and PMAn) with fast and reversible photoresponsive properties were prepared using rosin-based azobenzene groups and polyethylene glycol, respectively. Under 5-10 s of UV irradiation, the polymers showed trans-to-cis isomerization and reached a photosteady state. For the PAMn polymer, the absorbance of the absorption peak at 325 nm recovered to more than 95% of the initial value under visible light for 5- 10 s, whereas that of the PMAn polymer recovered completely. Notably, the PAMn and PMAn polymers initially self-assembled to vesicles or spherical micelles, and various morphological changes were achieved by manipulating UV irradiation time, with the initial morphology again recovered under dark conditions or visible-light irradiation. Remarkably, vesicles of the PAM34 and PMA34 polymers presented an intermediate open-vesicle state before being completely deformed under UV irradiation because of the existence of a pi-pi interaction. Finally, the ability of PAM34 and PMA34 polymer vesicles to perform the controlled release and reversible loading of a fluorescent probe was evaluated.
引用
收藏
页码:12885 / 12896
页数:12
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