Nanomedicine based potentially transformative strategies for colon targeting of peptides: State-of-the-art

被引:9
|
作者
Vambhurkar, Ganesh [1 ]
Amulya, Etikala [1 ]
Sikder, Anupama [1 ]
Shah, Saurabh [1 ]
Famta, Paras [1 ]
Khatri, Dharmendra Kumar [2 ]
Singh, Shashi Bala [2 ]
Srivastava, Saurabh [1 ,3 ]
机构
[1] Natl Inst Pharmaceut Educ & Res NIPER, Dept Pharmaceut, Hyderabad, India
[2] Natl Inst Pharmaceut Educ & Res NIPER, Dept Biol Sci, Hyderabad, India
[3] Natl Inst Pharmaceut Educ & Res NIPER, Dept Pharmaceut, Hyderabad 500037, Telangana, India
关键词
Colon -specific delivery; Peptides; Nanocarriers; Regulatory perspectives; Barriers; INFLAMMATORY-BOWEL-DISEASE; DRUG-DELIVERY; ORAL DELIVERY; GUT MICROBIOTA; NANOPARTICLES; INSULIN; PH; CHITOSAN; PROTEIN; LIPOSOMES;
D O I
10.1016/j.colsurfb.2022.112816
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Recently, peptides have attracted tremendous attention among researchers attributed to their high target spec-ificity and efficacy compared to conventional therapeutics. The ease of self-administration and non-invasiveness confers oral as the most desirable route. However, numerous challenges associated with peptide delivery through the oral route like harsh gastrointestinal environment, enzymatic degradation, and absorption barriers hinder its clinical translation. Protease activity is more pronounced in the proximal segments of the gastrointestinal tract (GIT). Distal segments like the colon possess lower proteolytic activity, enhanced retention time, etc. which could facilitate easy absorption. However, traversing of the upper segments to reach the colon requires the circum-vention of the pitfalls of the GIT. The advent of nanomedicine strategies could help in overcoming the said challenges associated with oral delivery, colon-specific targeting, and improving stability and bioavailability at the active site. Furthermore, the classification of peptides and various nanomedicine strategies for oral delivery of peptides to the colon has been conveyed. Regulatory hurdles and ways to accomplish clinical translation have been addressed.
引用
收藏
页数:14
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