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摘要:
The absorption of peptides and proteins delivered orally is minimum because of the intestine epithelial barrier.There are few known active transport mechanisms for macromolecules including the neonatal Fc Receptor(FcRn)for the absorption and secretion of IgGs in infant and adult intestine.We had previously described the FnAb-8 protein that could bind to h FcRn tightly at pH 6.0 but barely at pH 7.4.In this study,we examined its uptake,biodistribution and pharmacokinetics after peroral administration in both wild-type and human FcRn transgenic(Tg)mice.FnAb-8 was modified to contain trans-cyclooctene(TCO)which could interact with18 F labeled tetrazine in situ via the bioorthogonal inverseelectron-demand Diels-Alder reaction.We showed that FnAb-8 had a tendency to distribute and persist in the Tg mice intestine for an extended duration of time.It could also be absorbed into the circulation and distributed systemically over a long period of time up to 172 h.The improvement in oral uptake and concentration in the intestine tissue may be valuable for designing oral delivery of biopharmaceuticals,especially for diseases involving the gastric intestinal tissue.
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篇名 Oral uptake and persistence of the FnAb-8 protein characterized by in situ radio-labeling and PET/CT imaging
来源期刊 亚洲药物制剂科学(英文) 学科 医学
关键词 FCRN IEDDA Oral uptake
年,卷(期) 2020,(6) 所属期刊栏目
研究方向 页码范围 752-758
页数 7页 分类号 R73
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FCRN
IEDDA
Oral
uptake
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亚洲药物制剂科学(英文)
双月刊
1818-0876
21-1608/R
中国沈阳市文化路103号107号信箱
8-624
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70
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0
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0
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