Self-Assembly, Drug Encapsulation, and Cellular Uptake of Block and Gradient Copolymers of 2-Methyl-2-oxazine and 2-n-Propyl/butyl-2-oxazoline

2021 ◽  
Author(s):  
David Babuka ◽  
Kristyna Kolouchova ◽  
Lenka Loukotova ◽  
Ondrej Sedlacek ◽  
Ondrej Groborz ◽  
...  
2017 ◽  
Vol 50 (8) ◽  
pp. 3215-3223 ◽  
Author(s):  
Yusuke Ogura ◽  
Müge Artar ◽  
Anja R. A. Palmans ◽  
Mitsuo Sawamoto ◽  
E. W. Meijer ◽  
...  

2019 ◽  
Vol 20 (15) ◽  
pp. 3781 ◽  
Author(s):  
Tomonori Waku ◽  
Saki Nishigaki ◽  
Yuichi Kitagawa ◽  
Sayaka Koeda ◽  
Kazufumi Kawabata ◽  
...  

Recently, nanofibers (NFs) formed from antigenic peptides conjugated to β-sheet-forming peptides have attracted much attention as a new generation of vaccines. However, studies describing how the hydrophilic-hydrophobic balance of NF components affects cellular interactions of NFs are limited. In this report, three different NFs were prepared by self-assembly of β-sheet-forming peptides conjugated with model antigenic peptides (SIINFEKL) from ovalbumin and hydrophilic oligo-ethylene glycol (EG) of differing chain lengths (6-, 12- and 24-mer) to investigate the effect of EG length of antigen-loaded NFs on their cellular uptake, cytotoxicity, and dendritic cell (DC)-stimulation ability. We used an immortal DC line, termed JAWS II, derived from bone marrow-derived DCs of a C57BL/6 p53-knockout mouse. The uptake of NFs, consisting of the EG 12-mer by DCs, was the most effective and activated DC without exhibiting significant cytotoxicity. Increasing the EG chain length significantly reduced cellular entry and DC activation by NFs. Conversely, shortening the EG chain enhanced DC activation but increased toxicity and impaired water-dispersibility, resulting in low cellular uptake. These results show that the interaction of antigen-loaded NFs with cells can be tuned by the EG length, which provides useful design guidelines for the development of effective NF-based vaccines.


2020 ◽  
Vol 11 (42) ◽  
pp. 6794-6802
Author(s):  
Xiaofeng Guo ◽  
Tianren Zhang ◽  
Yuetong Wu ◽  
Wencheng Shi ◽  
Bonnie Choi ◽  
...  

Switchable RAFT agents, so-called because they can be reversibly switched by an acid/base stimulus to offer very good control over polymerization of both MAMs and LAMs, provide a route to prepare well-defined polyMAM-block-polyLAM copolymers.


2009 ◽  
Vol 78 (12) ◽  
pp. 1464-1474 ◽  
Author(s):  
Britta M. Folmer ◽  
Denis Barron ◽  
Eric Hughes ◽  
Laurence Miguet ◽  
Belén Sanchez ◽  
...  

2015 ◽  
Vol 137 (32) ◽  
pp. 10040-10043 ◽  
Author(s):  
Jie Zhou ◽  
Xuewen Du ◽  
Jie Li ◽  
Natsuko Yamagata ◽  
Bing Xu

2010 ◽  
Vol 47 (8) ◽  
pp. 788-793 ◽  
Author(s):  
Mukesh K. Pandey ◽  
Ke Yang ◽  
Cao Pei ◽  
Pramod K. Sharma ◽  
Joana Viola ◽  
...  

2018 ◽  
Vol 9 (15) ◽  
pp. 2002-2010 ◽  
Author(s):  
Junxian Chen ◽  
Bowen Li ◽  
Xiaofu Li ◽  
Jie Zhang ◽  
Xinhua Wan

A series of novel gradient copolymers R-(−)-poly(StN-grad-C8) were synthesized through atom transfer radical copolymerization of an achiral styrenic monomer, N,N-dimethyl-4-ethenylbenzamide (M-StN), and a chiral bulky vinylterphenyl monomer, (−)-2,5-bis{4′-[(R)-sec-octyloxycarbonyl]phenyl}styrene (R-(−)-M-C8).


2015 ◽  
Vol 3 (17) ◽  
pp. 3425-3428 ◽  
Author(s):  
Nagaraj Nayak ◽  
Karical R. Gopidas

A hydrophilic β-cyclodextrin bis-inclusion complex forms supramolecular vesicles which can be loaded with the anti-cancer drug doxorubicin. The loaded drug can be released upon addition of a competitive inclusion binder such as adamantane carboxylate.


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