1406-P: ZP8396, a Novel Amylin Analogue, Induces Weight Loss in DIO Rats with a Formulation Space at Physiological pH

减肥 胰淀素 加药 等渗 药理学 医学 化学 体内 内科学 动物科学 内分泌学 肥胖 糖尿病 生物 生物技术 小岛
作者
JOLANTA SKARBALIENE,JOAKIM LUNDQVIST,Jesper Skodborg Villadsen
出处
期刊:Diabetes [American Diabetes Association]
卷期号:71 (Supplement_1) 被引量:1
标识
DOI:10.2337/db22-1406-p
摘要

ZP8396, currently in phase 1, is a long-acting, amylin analogue designed to improve solubility and stability and allow for co-formulation with other peptides at physiological pH. Here we present in-vivo efficacy and formulation design space of ZP8396. The acute effects on body weight (BW) loss after a single s.c. injection of ZP8396 (0,5, 3, 30, 300 nmol/kg) were measured in lean rats and monitored for 96 hours after dosing. The ability of ZP8396 (1, 3, and 15 nmol/kg, s.c., every 2nd day for 21 days) to reduce BW was tested in diet-induced obese (DIO) rats. ZP8396, at concentration supporting pharmacological relevant human doses, is stable in an aqueous formulation at neutral pH and shows no aggregation potential. ZP8396 is compatible with different physiological buffer systems and isotonic agents, commonly used for commercial medicinal products (Table 1) . Formulation of ZP8396 at physiological pH induces a significant BW loss in both lean and DIO rats vs. vehicle group. A significant BW loss was observed from start of the dosing and throughout the study period. In conclusion, ZP8396 potently induces BW loss in lean and DIO rats and allows for aqueous stable formulation at neutral pH which provides opportunities for co-formulation with other peptides for optimal BW loss. Further preclinical characterization of co-formulation of ZP8396 with different peptides for weight management is ongoing. Disclosure J.Skarbaliene: Employee; Zealand Pharma A/S, Stock/Shareholder; Zealand Pharma A/S. J.Lundqvist: Employee; Zealand Pharma A/S. J.Villadsen: Employee; Zealand Pharma A/S.

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
思维隋发布了新的文献求助10
刚刚
lzp发布了新的文献求助10
1秒前
fd163c应助sci帝国采纳,获得10
1秒前
黑熊安巴尼完成签到,获得积分20
1秒前
anmeiii完成签到,获得积分10
2秒前
田様应助神棍喜来乐采纳,获得10
3秒前
4秒前
风中垣完成签到,获得积分10
4秒前
anmeiii发布了新的文献求助10
5秒前
有魅力的乐珍完成签到 ,获得积分10
5秒前
Owen应助诸葛钢铁采纳,获得10
6秒前
Eliauk发布了新的文献求助10
6秒前
7秒前
9秒前
lzp完成签到,获得积分10
10秒前
10秒前
kkeyanxiaozi发布了新的文献求助10
13秒前
解语花应助Hanxi采纳,获得30
13秒前
Orange应助回鱼采纳,获得10
13秒前
wangei198728关注了科研通微信公众号
13秒前
14秒前
wy.he应助千千千千千千青采纳,获得20
14秒前
15秒前
16秒前
17秒前
17秒前
DYYDYY发布了新的文献求助10
18秒前
renshiq完成签到,获得积分10
18秒前
mnliao完成签到,获得积分10
18秒前
木木应助lyl采纳,获得10
18秒前
Hello应助黑熊安巴尼采纳,获得10
19秒前
噜噜发布了新的文献求助10
20秒前
20秒前
21秒前
22秒前
22秒前
khaosyi完成签到 ,获得积分10
22秒前
思源应助诺曼采纳,获得10
24秒前
24秒前
24秒前
高分求助中
Picture Books with Same-sex Parented Families: Unintentional Censorship 1000
A new approach to the extrapolation of accelerated life test data 1000
ACSM’s Guidelines for Exercise Testing and Prescription, 12th edition 500
Nucleophilic substitution in azasydnone-modified dinitroanisoles 500
Indomethacinのヒトにおける経皮吸収 400
Phylogenetic study of the order Polydesmida (Myriapoda: Diplopoda) 370
基于可调谐半导体激光吸收光谱技术泄漏气体检测系统的研究 310
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3979788
求助须知:如何正确求助?哪些是违规求助? 3523806
关于积分的说明 11218898
捐赠科研通 3261339
什么是DOI,文献DOI怎么找? 1800544
邀请新用户注册赠送积分活动 879177
科研通“疑难数据库(出版商)”最低求助积分说明 807182