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新型醋酸戈舍瑞林缓释微球在大鼠体内的药理毒理学研究

Pharmacological and toxicological studies of a novel goserelin acetate extended-release microspheres in rats.

作者信息

Yutong Mao, Liang Ye, Chunjie Sha, Xiaolin Guan, Xiaoyan Gong, Lin Dong, Guangying Du, Xuemei Zhang, Xiaobo Cen, Jingwei Tian, Pengfei Yu, Hongbo Wang

机构信息

School of Pharmacy, Key Laboratory of Molecular Pharmacology and Drug Evaluation (Yantai University), Ministry of Education, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong, Yantai University, Yantai, China.

School of Pharmacy, Binzhou Medical University, Yantai, China.

出版信息

Front Pharmacol. 2023 Feb 21;14:1125255. doi: 10.3389/fphar.2023.1125255. eCollection 2023.

DOI:10.3389/fphar.2023.1125255
PMID:36895949
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9989164/
Abstract

LY01005 is an investigational new drug product of goserelin acetate which is formulated as extended-release microspheres for intramuscular injection. To support the proposed clinical trials and marketing application of LY01005, pharmacodynamics, pharmacokinetics and toxicity studies were performed in rats. In the pharmacological study in rats, LY01005 induced an initial supra-physiological level increase of testosterone at 24 h post-dosing which then rapidly fell to castration level. The potency of LY01005 was comparable to the comparator Zoladex but its effect lasted longer and more stable. A single-dose pharmacokinetics study in rats demonstrated that the C and AUC of LY01005 increased in a dose-proportional manner in the range of 0.45-1.80 mg/kg and the relative bioavailability was 101.0% between LY01005 and Zoladex. In the toxicity study, almost all of the positive findings of LY01005 in rats including the changes in hormones (follicle-stimulating hormone, luteinizing hormone, testosterone, progestin) and in reproductive system (uterus, ovary, vagina, cervix uteri, mammary gland, testis, epididymis and prostate) were related to the direct pharmacological effects of goserelin. Mild histopathological changes in foreign body removal reaction induced by excipient were also observed. In conclusion, LY01005 displayed a sustained-release profile of goserelin, and exerted a continuous efficacy in animal models, which had a comparable potency but with a more sustained effect than that of Zoladex. The safety profile of LY01005 was largely the same with Zoladex. These results strongly support the planned LY01005 clinical trials.

摘要

LY01005是一种醋酸戈舍瑞林的研究用新药产品,其剂型为用于肌肉注射的缓释微球。为支持LY01005拟进行的临床试验和上市申请,在大鼠中开展了药效学、药代动力学和毒性研究。在大鼠的药理学研究中,LY01005在给药后24小时诱导睾酮出现初始超生理水平升高,随后迅速降至去势水平。LY01005的效力与对照药诺雷德相当,但其作用持续时间更长且更稳定。大鼠单剂量药代动力学研究表明,LY01005的Cmax和AUC在0.45 - 1.80mg/kg范围内呈剂量比例增加,LY01005与诺雷德之间的相对生物利用度为101.0%。在毒性研究中,LY01005在大鼠中的几乎所有阳性发现,包括激素(促卵泡激素、促黄体生成素、睾酮、孕激素)和生殖系统(子宫、卵巢、阴道、子宫颈、乳腺、睾丸、附睾和前列腺)的变化,均与戈舍瑞林的直接药理作用有关。还观察到由辅料引起的轻度组织病理学异物清除反应变化。总之,LY01005呈现出戈舍瑞林的缓释特征,并在动物模型中发挥持续疗效,其效力与诺雷德相当,但效果更持久。LY01005的安全性概况与诺雷德基本相同。这些结果有力地支持了LY01005的计划临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c0b/9989164/71c30a00534a/fphar-14-1125255-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c0b/9989164/c38f41efe10f/fphar-14-1125255-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c0b/9989164/107e02855e59/fphar-14-1125255-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c0b/9989164/b6e556b19b77/fphar-14-1125255-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c0b/9989164/2ea901668ec6/fphar-14-1125255-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c0b/9989164/71c30a00534a/fphar-14-1125255-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c0b/9989164/c38f41efe10f/fphar-14-1125255-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c0b/9989164/107e02855e59/fphar-14-1125255-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c0b/9989164/b6e556b19b77/fphar-14-1125255-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c0b/9989164/2ea901668ec6/fphar-14-1125255-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c0b/9989164/71c30a00534a/fphar-14-1125255-g005.jpg

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本文引用的文献

1
Hormonal Therapy for Prostate Cancer.前列腺癌的激素治疗。
Endocr Rev. 2021 May 25;42(3):354-373. doi: 10.1210/endrev/bnab002.
2
Clinical pharmacology and regulatory consequences of GnRH analogues in prostate cancer.GnRH类似物在前列腺癌中的临床药理学及监管影响
Eur J Clin Pharmacol. 2014 Jul;70(7):791-8. doi: 10.1007/s00228-014-1682-1. Epub 2014 Apr 23.
3
[Effect of local cooling at injection site of goserelin acetate for pain relief].[醋酸戈舍瑞林注射部位局部冷敷对缓解疼痛的作用]
Gan To Kagaku Ryoho. 2011 Jun;38(6):967-72.
4
Effective testosterone suppression for prostate cancer: is there a best castration therapy?前列腺癌的有效睾酮抑制:是否存在最佳去势疗法?
Rev Urol. 2009 Spring;11(2):52-60.
5
Antitumor activity with CYP17 blockade indicates that castration-resistant prostate cancer frequently remains hormone driven.CYP17阻断的抗肿瘤活性表明,去势抵抗性前列腺癌通常仍由激素驱动。
Cancer Res. 2009 Jun 15;69(12):4937-40. doi: 10.1158/0008-5472.CAN-08-4531. Epub 2009 Jun 9.
6
Effects of reduced food intake on toxicity study parameters in rats.食物摄入量减少对大鼠毒性研究参数的影响。
J Toxicol Sci. 2008 Dec;33(5):537-47. doi: 10.2131/jts.33.537.
7
Design and end points of clinical trials for patients with progressive prostate cancer and castrate levels of testosterone: recommendations of the Prostate Cancer Clinical Trials Working Group.进展性前列腺癌和睾酮去势水平患者的临床试验设计与终点:前列腺癌临床试验工作组的建议
J Clin Oncol. 2008 Mar 1;26(7):1148-59. doi: 10.1200/JCO.2007.12.4487.
8
Goserelin: a review of its use in the treatment of early breast cancer in premenopausal and perimenopausal women.戈舍瑞林:用于治疗绝经前和围绝经期妇女早期乳腺癌的综述
Drugs. 2005;65(18):2639-55. doi: 10.2165/00003495-200565180-00011.
9
Failure to achieve castration levels in patients using leuprolide acetate in locally advanced prostate cancer.在局部晚期前列腺癌患者中使用醋酸亮丙瑞林未能达到去势水平。
Eur Urol. 2006 Jan;49(1):54-8; discussion 58. doi: 10.1016/j.eururo.2005.09.009. Epub 2005 Nov 15.
10
Serum testosterone suppression and potential for agonistic stimulation during chronic treatment with monthly and 3-month depot formulations of leuprolide acetate for advanced prostate cancer.
J Urol. 2002 Sep;168(3):1001-4. doi: 10.1016/S0022-5347(05)64560-0.