Glyoxylamide-based self-assembly hydrogels for sustained ciprofloxacin delivery

被引:17
作者
Aldilla, Vina R. [1 ]
Martin, Adam D. [1 ,2 ,3 ]
Nizalapur, Shashidhar [1 ]
Marjo, Christopher E. [4 ]
Rich, Anne M. [4 ]
Ho, Kitty K. K. [1 ]
Ittner, Lars M. [5 ,6 ]
Black, David StC. [1 ]
Thordarson, Pall [1 ,2 ,3 ]
Kumar, Naresh [1 ,2 ,3 ]
机构
[1] UNSW, Sch Chem, Sydney, NSW 2052, Australia
[2] Univ New South Wales, Australian Ctr Nanomed, Sydney, NSW 2052, Australia
[3] Univ New South Wales, ARC Ctr Excellence Convergent Bionano Sci & Techn, Sydney, NSW 2052, Australia
[4] UNSW, Mark Wainwright Analyt Ctr, Sydney, NSW 2052, Australia
[5] UNSW, Sch Med Sci, Dementia Res Unit, Sydney, NSW 2052, Australia
[6] Macquarie Univ, Fac Med & Hlth Sci, Dementia Res Ctr, N Ryde, NSW 2109, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
DIPHENYLALANINE PEPTIDE NANOTUBES; DRUG-DELIVERY; SUPRAMOLECULAR HYDROGEL; POTENTIAL APPLICATION; INJECTABLE HYDROGEL; DESIGN; ANTIBIOTICS; TRIPEPTIDE; QUINOLONE; CHITOSAN;
D O I
10.1039/c8tb01290c
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
In this study, we report the synthesis of glyoxylamide peptide-mimics as self-assembled gels with well-defined molecular structures for topical delivery of ciprofloxacin (CIP). The glyoxylamide peptide mimics successfully formed hydrogels with critical gel concentrations of 0.02-0.08% (w/v). The mechanical strength, secondary structure, and fiber morphology of these hydrogels can be modulated by varying the N-substituent of the ring-opened isatins. The synthesised hydrogel exhibited a high loading capacity of CIP (40% (w/w)) and a sustained release profile. The CIP-loaded hydrogels were able to release CIP for more than 15 days and the released solution was shown to retain activity against Gram-positive and Gram-negative bacteria. In addition, the hydrogels formed showed low toxicity against Cos7 cells.
引用
收藏
页码:6089 / 6098
页数:10
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