Amphiphilic conjugates of human brain natriuretic peptide designed for oral delivery: In vitro activity screening

被引:14
作者
Miller, MA [1 ]
Malkar, NB [1 ]
Severynse-Stevens, D [1 ]
Yarbrough, KG [1 ]
Bednarcik, MJ [1 ]
Dugdell, RE [1 ]
Puskas, ME [1 ]
Krishnan, R [1 ]
James, KD [1 ]
机构
[1] Nobex Corp, Durham, NC 27713 USA
关键词
D O I
10.1021/bc0501000
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Congestive heart failure (CHF) is a complex syndrome involving altered neurohormonal levels and impaired cardiac and renal function. In recent years, intravenous administration of exogenous human brain-type natriuretic peptide (hBNP) has become an important therapy in treating patients with acutely decompensated CHF. However, reports during the past year suggest that hBNP could play a prominent role in the chronic treatment of CHF patients as well. We are Currently developing conjugates of hBNP suitable for oral delivery to provide a patient-friendly treatment option for chronic heart failure patients. In this report, we present in vitro activity results obtained from hBNP conjugates featuring a variety of rationally designed amphiphilic oligomers. Mapping studies revealed that the hydrophobic/hydrophilic balance of the oligomer impacted the regioselectivity of conjugation. Additionally, the regiochemistry and extent of conjugation had a significant impact on activity. Many monoconjugates retained activity comparable to native peptide and are currently under evaluation in subsequent in vivo screens.
引用
收藏
页码:267 / 274
页数:8
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