دورية أكاديمية

Evaluation of Toxic Properties of New Glycopeptide Flavancin on Rats.

التفاصيل البيبلوغرافية
العنوان: Evaluation of Toxic Properties of New Glycopeptide Flavancin on Rats.
المؤلفون: Treshchalin MI; Gause Institute of New Antibiotics, 11 B. Pirogovskaya Street, 119021 Moscow, Russia., Polozkova VA; Gause Institute of New Antibiotics, 11 B. Pirogovskaya Street, 119021 Moscow, Russia., Moiseenko EI; Gause Institute of New Antibiotics, 11 B. Pirogovskaya Street, 119021 Moscow, Russia., Treshalina HM; Gause Institute of New Antibiotics, 11 B. Pirogovskaya Street, 119021 Moscow, Russia., Shchekotikhin AE; Gause Institute of New Antibiotics, 11 B. Pirogovskaya Street, 119021 Moscow, Russia.; Organic Chemistry Department, Mendeleyev University of Chemical Technology of Russia, 9 Miusskaya Square, 125047 Moscow, Russia., Pereverzeva ER; Gause Institute of New Antibiotics, 11 B. Pirogovskaya Street, 119021 Moscow, Russia.
المصدر: Pharmaceuticals (Basel, Switzerland) [Pharmaceuticals (Basel)] 2022 May 25; Vol. 15 (6). Date of Electronic Publication: 2022 May 25.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101238453 Publication Model: Electronic Cited Medium: Print ISSN: 1424-8247 (Print) Linking ISSN: 14248247 NLM ISO Abbreviation: Pharmaceuticals (Basel) Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: Basel, Switzerland : MDPI, c2004-
مستخلص: Glycopeptide antibiotics have side effects that limit their clinical use. In view of this, the development of glycopeptides with improved chemotherapeutic properties remains the main direction in the search for new antibacterial drugs. The objective of this study was to evaluate the toxicological characteristics of new semi-synthetic glycopeptide flavancin. Acute and chronic toxicity of antibiotic was evaluated in Wistar rats. The medium lethal dose (LD 50 ) and the maximum tolerated doses (MTD) were calculated by the method of Litchfield and Wilcoxon. In the chronic toxicity study, the treatment regimen consisted of 15 daily intraperitoneal injections using two dosage levels: 6 and 10 mg/kg/day. Total doses were equivalent to MTD or LD 50 of flavancin, respectively. The study included assessment of the body weight, hematological parameters, blood biochemical parameters, urinalysis, and pathomorphological evaluation of the internal organs. The results of the study demonstrated that no clinical-laboratory signs of toxicity were found after 15 daily injections of flavancin at a total dose close to the MTD or LD 50 . The pathomorphological study did not reveal any lesions on the organ structure of animals after low-dose administration of flavancin. Thus, flavancin favorably differs in terms of toxicological properties from the glycopeptides currently used in the clinic.
References: J Med Chem. 2002 Mar 14;45(6):1340-7. (PMID: 11882003)
Antibiot Khimioter. 1989 Jan;34(1):52-6. (PMID: 2543344)
Pharmaceuticals (Basel). 2021 Apr 19;14(4):. (PMID: 33921612)
Front Public Health. 2014 Oct 31;2:217. (PMID: 25401098)
Environ Toxicol Chem. 2016 Dec;35(12):3058-3061. (PMID: 27175944)
Future Med Chem. 2013 Apr;5(6):641-52. (PMID: 23617428)
Antibiot Med Biotekhnol. 1987 Aug;32(8):571-6. (PMID: 3674837)
Braz J Infect Dis. 2002 Aug;6(4):196-200. (PMID: 12204187)
Am Fam Physician. 2003 Nov 1;68(9):1781-90. (PMID: 14620598)
J Antibiot (Tokyo). 2007 Apr;60(4):245-50. (PMID: 17456974)
Expert Opin Drug Saf. 2010 Jan;9(1):9-14. (PMID: 20021290)
Antibiot Khimioter. 1988 Apr;33(4):280-6. (PMID: 3389957)
Antibiot Khimioter. 1989 Mar;34(3):209-12. (PMID: 2473716)
ACS Infect Dis. 2021 Sep 10;7(9):2746-2754. (PMID: 34387988)
ACS Infect Dis. 2018 May 11;4(5):715-735. (PMID: 29363950)
Int J Antimicrob Agents. 2016 Nov;48(5):528-534. (PMID: 27665522)
J Med Chem. 2007 Jul 26;50(15):3681-5. (PMID: 17608397)
Pharmaceuticals (Basel). 2021 Jan 22;14(2):. (PMID: 33499349)
Int J Antimicrob Agents. 2015 Mar;45(3):213-20. (PMID: 25600892)
Can J Microbiol. 2020 Jan;66(1):11-16. (PMID: 31545906)
Drug Des Devel Ther. 2018 Sep 10;12:2875-2885. (PMID: 30237697)
Chem Commun (Camb). 2022 Feb 8;58(12):1881-1897. (PMID: 35043130)
Int J Antimicrob Agents. 2016 Jun;47(6):495-9. (PMID: 27211209)
Pharmacotherapy. 2001 Oct;21(10):1233-9. (PMID: 11601669)
Antibiot Khimioter. 1989 Jul;34(7):523-6. (PMID: 2530944)
ACS Infect Dis. 2020 Aug 14;6(8):2169-2180. (PMID: 32598127)
Ann Pharmacother. 2011 May;45(5):629-38. (PMID: 21521866)
فهرسة مساهمة: Keywords: acute toxicity; chronic toxicity; eremomycin; flavancin; rats; semi-synthetic glycopeptide antibiotics; vancomycin
تواريخ الأحداث: Date Created: 20220624 Latest Revision: 20220716
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC9228439
DOI: 10.3390/ph15060661
PMID: 35745578
قاعدة البيانات: MEDLINE
الوصف
تدمد:1424-8247
DOI:10.3390/ph15060661