I. Tsvetkov, N. Zolotova, A. Kosyreva, D. Dzhalilova, V. Kudelkina, V. Chernikov, V. Mkhitarov, L. Mikhailova, N. Soboleva, V. Razzhivina, M. Dobrynina, S. Gelperina, O. Makarova
{"title":"阿霉素和阿霉素plga纳米颗粒肾毒性的形态学特征","authors":"I. Tsvetkov, N. Zolotova, A. Kosyreva, D. Dzhalilova, V. Kudelkina, V. Chernikov, V. Mkhitarov, L. Mikhailova, N. Soboleva, V. Razzhivina, M. Dobrynina, S. Gelperina, O. Makarova","doi":"10.31088/cem2021.10.s4.77-86","DOIUrl":null,"url":null,"abstract":"Introduction. Doxorubicin is an anticancer chemotherapy drug that has cardiotoxic, hepatotoxic, and nephrotoxic effects. To reduce the toxic effects of doxorubicin, its nanosomal form, PLGA-doxorubicin [Poly(Lactic-co-Glycolic Acid)], has been developed. PLGA is a biodegradable polymer used as a drug delivery system. The nephrotoxic effects of PLGA-doxorubicin have not been studied yet. The aim was to compare the nephrotoxic effects of therapeutic doses of doxorubicin in standard form (Dox) and PLGA-doxorubicin (PLGA-Dox). Materials and methods. Mature male Wistar rats were injected intravenously three times with Dox or PLGA-Dox solution, at a therapeutic dose of 1.75 mg/kg. The animals were sacrificed on days 8 and 21. We carried out morphological, histochemical, and ultrastructural studies of the kidneys. Results. Under the influence of Dox or PLGA-Dox in the kidneys on days 8 and 21 of the experiment, histological and ultrastructural examination revealed dystrophic changes in the proximal tubules with the destruction of the brush border; in the distal tubules and collecting ducts, protein cylinders were located. Dystrophic changes were more pronounced on day 21 than on day 8. During both periods of the experiment, PLGA-Dox caused less pronounced dystrophic changes in the epithelium than Dox that is confirmed by a morphometric assessment of the number of proximal tubules with a destroyed brush border. Conclusion. The nanosomal PLGA-doxorubicin form has a less pronounced nephrotoxic effect than the classical form of doxorubicin. Keywords: nephrotoxic effect, doxorubicin, nanoparticles, PLGA, morphology","PeriodicalId":36062,"journal":{"name":"Clinical and Experimental Morphology","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Morphological characteristics of nephrotoxicity of doxorubicin and doxorubicin PLGA-nanoparticles\",\"authors\":\"I. Tsvetkov, N. Zolotova, A. Kosyreva, D. Dzhalilova, V. Kudelkina, V. Chernikov, V. Mkhitarov, L. Mikhailova, N. Soboleva, V. Razzhivina, M. Dobrynina, S. Gelperina, O. Makarova\",\"doi\":\"10.31088/cem2021.10.s4.77-86\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction. Doxorubicin is an anticancer chemotherapy drug that has cardiotoxic, hepatotoxic, and nephrotoxic effects. To reduce the toxic effects of doxorubicin, its nanosomal form, PLGA-doxorubicin [Poly(Lactic-co-Glycolic Acid)], has been developed. PLGA is a biodegradable polymer used as a drug delivery system. The nephrotoxic effects of PLGA-doxorubicin have not been studied yet. The aim was to compare the nephrotoxic effects of therapeutic doses of doxorubicin in standard form (Dox) and PLGA-doxorubicin (PLGA-Dox). Materials and methods. Mature male Wistar rats were injected intravenously three times with Dox or PLGA-Dox solution, at a therapeutic dose of 1.75 mg/kg. The animals were sacrificed on days 8 and 21. We carried out morphological, histochemical, and ultrastructural studies of the kidneys. Results. Under the influence of Dox or PLGA-Dox in the kidneys on days 8 and 21 of the experiment, histological and ultrastructural examination revealed dystrophic changes in the proximal tubules with the destruction of the brush border; in the distal tubules and collecting ducts, protein cylinders were located. Dystrophic changes were more pronounced on day 21 than on day 8. During both periods of the experiment, PLGA-Dox caused less pronounced dystrophic changes in the epithelium than Dox that is confirmed by a morphometric assessment of the number of proximal tubules with a destroyed brush border. Conclusion. The nanosomal PLGA-doxorubicin form has a less pronounced nephrotoxic effect than the classical form of doxorubicin. Keywords: nephrotoxic effect, doxorubicin, nanoparticles, PLGA, morphology\",\"PeriodicalId\":36062,\"journal\":{\"name\":\"Clinical and Experimental Morphology\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical and Experimental Morphology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.31088/cem2021.10.s4.77-86\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical and Experimental Morphology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31088/cem2021.10.s4.77-86","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
Morphological characteristics of nephrotoxicity of doxorubicin and doxorubicin PLGA-nanoparticles
Introduction. Doxorubicin is an anticancer chemotherapy drug that has cardiotoxic, hepatotoxic, and nephrotoxic effects. To reduce the toxic effects of doxorubicin, its nanosomal form, PLGA-doxorubicin [Poly(Lactic-co-Glycolic Acid)], has been developed. PLGA is a biodegradable polymer used as a drug delivery system. The nephrotoxic effects of PLGA-doxorubicin have not been studied yet. The aim was to compare the nephrotoxic effects of therapeutic doses of doxorubicin in standard form (Dox) and PLGA-doxorubicin (PLGA-Dox). Materials and methods. Mature male Wistar rats were injected intravenously three times with Dox or PLGA-Dox solution, at a therapeutic dose of 1.75 mg/kg. The animals were sacrificed on days 8 and 21. We carried out morphological, histochemical, and ultrastructural studies of the kidneys. Results. Under the influence of Dox or PLGA-Dox in the kidneys on days 8 and 21 of the experiment, histological and ultrastructural examination revealed dystrophic changes in the proximal tubules with the destruction of the brush border; in the distal tubules and collecting ducts, protein cylinders were located. Dystrophic changes were more pronounced on day 21 than on day 8. During both periods of the experiment, PLGA-Dox caused less pronounced dystrophic changes in the epithelium than Dox that is confirmed by a morphometric assessment of the number of proximal tubules with a destroyed brush border. Conclusion. The nanosomal PLGA-doxorubicin form has a less pronounced nephrotoxic effect than the classical form of doxorubicin. Keywords: nephrotoxic effect, doxorubicin, nanoparticles, PLGA, morphology