共 68 条
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.
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页码:6089 / 6098
页数:10
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