Oral treatment of spontaneously hypertensive rats with captopril-surface functionalized furosemide-loaded multi-wall lipid-core nanocapsules
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/231510 |
Resumo: | Multi-wall lipid-core nanocapsule (MLNC) functionalized with captopril and nanoencapsulating furosemide within the core was developed as a liquid formulation for oral administration. The nanocapsules had mean particle size below 200 nm, showing unimodal and narrow size distributions with moderate dispersity (laser di raction and dynamic light scattering). Zeta potential was inverted from 14.3 mV [LNC-Fur(0,5)] to +18.3 mV after chitosan coating. Transmission electron microscopy and atomic force microscopy showed spherical structures corroborating the nanometric diameter of the nanocapsules. Regarding the systolic pressure, on the first day, the formulations showed antihypertensive e ect and a longer e ect than the respective drug solutions. When both drugs were associated, the anti-hypertensive e ect was prolonged. On the fifth day, a time e ect reduction was observed for all treatments, except for the nanocapsule formulation containing both drugs [Capt(0.5)-Zn(25)-MLNC-Fur(0.45)]. For diastolic pressure, only Capt(0.5)-Zn(25)-MLNC-Fur(0.45) presented a significant di erence (p < 0.05) on the first day. On the fifth day, both Capt(0.5)-MLNC-Fur(0.45) and Capt(0.5)-Zn(25)-MLNC-Fur(0.45) had an e ect lasting up to 24 h. The analysis of early kidney damage marker showed a potential protection in renal function by Capt(0.5)-Zn(25)-MLNC-Fur(0.45). In conclusion, the formulation Capt(0.5)-Zn(25)-MLNC-Fur(0.45) proved to be suitable for hypertension treatment envisaging an important innovation. |
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Michalowski, Cecilia BohnsArbo, Marcelo DutraAltknecht, Louise FigueredoAnciuti, Andréia NobreAbreu, Angélica Samara GonçalvesAlencar, Luciana Magalhães RebêloPohlmann, Adriana RaffinGarcia, Solange CristinaGuterres, Silvia Stanisçuaski2021-11-04T04:23:52Z20201999-4923http://hdl.handle.net/10183/231510001127987Multi-wall lipid-core nanocapsule (MLNC) functionalized with captopril and nanoencapsulating furosemide within the core was developed as a liquid formulation for oral administration. The nanocapsules had mean particle size below 200 nm, showing unimodal and narrow size distributions with moderate dispersity (laser di raction and dynamic light scattering). Zeta potential was inverted from 14.3 mV [LNC-Fur(0,5)] to +18.3 mV after chitosan coating. Transmission electron microscopy and atomic force microscopy showed spherical structures corroborating the nanometric diameter of the nanocapsules. Regarding the systolic pressure, on the first day, the formulations showed antihypertensive e ect and a longer e ect than the respective drug solutions. When both drugs were associated, the anti-hypertensive e ect was prolonged. On the fifth day, a time e ect reduction was observed for all treatments, except for the nanocapsule formulation containing both drugs [Capt(0.5)-Zn(25)-MLNC-Fur(0.45)]. For diastolic pressure, only Capt(0.5)-Zn(25)-MLNC-Fur(0.45) presented a significant di erence (p < 0.05) on the first day. On the fifth day, both Capt(0.5)-MLNC-Fur(0.45) and Capt(0.5)-Zn(25)-MLNC-Fur(0.45) had an e ect lasting up to 24 h. The analysis of early kidney damage marker showed a potential protection in renal function by Capt(0.5)-Zn(25)-MLNC-Fur(0.45). In conclusion, the formulation Capt(0.5)-Zn(25)-MLNC-Fur(0.45) proved to be suitable for hypertension treatment envisaging an important innovation.application/pdfengPharmaceutics. Basel. Vol. 12, n. 1 (2020), 80, 23 p.NanocápsulasAnti-hipertensivosCaptoprilFurosemidaLipid-core nanocapsulesAntihypertensiveSurface-functionalizationFurosemideToxicityOral drug deliveryOral treatment of spontaneously hypertensive rats with captopril-surface functionalized furosemide-loaded multi-wall lipid-core nanocapsulesEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001127987.pdf.txt001127987.pdf.txtExtracted Texttext/plain103384http://www.lume.ufrgs.br/bitstream/10183/231510/2/001127987.pdf.txt96481efad2d7f7d75518936a8b2a5ce2MD52ORIGINAL001127987.pdfTexto completo (inglês)application/pdf8476559http://www.lume.ufrgs.br/bitstream/10183/231510/1/001127987.pdf7541f83f2e967e38167be3e4ad19ae5bMD5110183/2315102021-11-20 05:47:31.991882oai:www.lume.ufrgs.br:10183/231510Repositório InstitucionalPUBhttps://lume.ufrgs.br/oai/requestlume@ufrgs.bropendoar:2021-11-20T07:47:31Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Oral treatment of spontaneously hypertensive rats with captopril-surface functionalized furosemide-loaded multi-wall lipid-core nanocapsules |
title |
Oral treatment of spontaneously hypertensive rats with captopril-surface functionalized furosemide-loaded multi-wall lipid-core nanocapsules |
spellingShingle |
Oral treatment of spontaneously hypertensive rats with captopril-surface functionalized furosemide-loaded multi-wall lipid-core nanocapsules Michalowski, Cecilia Bohns Nanocápsulas Anti-hipertensivos Captopril Furosemida Lipid-core nanocapsules Antihypertensive Surface-functionalization Furosemide Toxicity Oral drug delivery |
title_short |
Oral treatment of spontaneously hypertensive rats with captopril-surface functionalized furosemide-loaded multi-wall lipid-core nanocapsules |
title_full |
Oral treatment of spontaneously hypertensive rats with captopril-surface functionalized furosemide-loaded multi-wall lipid-core nanocapsules |
title_fullStr |
Oral treatment of spontaneously hypertensive rats with captopril-surface functionalized furosemide-loaded multi-wall lipid-core nanocapsules |
title_full_unstemmed |
Oral treatment of spontaneously hypertensive rats with captopril-surface functionalized furosemide-loaded multi-wall lipid-core nanocapsules |
title_sort |
Oral treatment of spontaneously hypertensive rats with captopril-surface functionalized furosemide-loaded multi-wall lipid-core nanocapsules |
author |
Michalowski, Cecilia Bohns |
author_facet |
Michalowski, Cecilia Bohns Arbo, Marcelo Dutra Altknecht, Louise Figueredo Anciuti, Andréia Nobre Abreu, Angélica Samara Gonçalves Alencar, Luciana Magalhães Rebêlo Pohlmann, Adriana Raffin Garcia, Solange Cristina Guterres, Silvia Stanisçuaski |
author_role |
author |
author2 |
Arbo, Marcelo Dutra Altknecht, Louise Figueredo Anciuti, Andréia Nobre Abreu, Angélica Samara Gonçalves Alencar, Luciana Magalhães Rebêlo Pohlmann, Adriana Raffin Garcia, Solange Cristina Guterres, Silvia Stanisçuaski |
author2_role |
author author author author author author author author |
dc.contributor.author.fl_str_mv |
Michalowski, Cecilia Bohns Arbo, Marcelo Dutra Altknecht, Louise Figueredo Anciuti, Andréia Nobre Abreu, Angélica Samara Gonçalves Alencar, Luciana Magalhães Rebêlo Pohlmann, Adriana Raffin Garcia, Solange Cristina Guterres, Silvia Stanisçuaski |
dc.subject.por.fl_str_mv |
Nanocápsulas Anti-hipertensivos Captopril Furosemida |
topic |
Nanocápsulas Anti-hipertensivos Captopril Furosemida Lipid-core nanocapsules Antihypertensive Surface-functionalization Furosemide Toxicity Oral drug delivery |
dc.subject.eng.fl_str_mv |
Lipid-core nanocapsules Antihypertensive Surface-functionalization Furosemide Toxicity Oral drug delivery |
description |
Multi-wall lipid-core nanocapsule (MLNC) functionalized with captopril and nanoencapsulating furosemide within the core was developed as a liquid formulation for oral administration. The nanocapsules had mean particle size below 200 nm, showing unimodal and narrow size distributions with moderate dispersity (laser di raction and dynamic light scattering). Zeta potential was inverted from 14.3 mV [LNC-Fur(0,5)] to +18.3 mV after chitosan coating. Transmission electron microscopy and atomic force microscopy showed spherical structures corroborating the nanometric diameter of the nanocapsules. Regarding the systolic pressure, on the first day, the formulations showed antihypertensive e ect and a longer e ect than the respective drug solutions. When both drugs were associated, the anti-hypertensive e ect was prolonged. On the fifth day, a time e ect reduction was observed for all treatments, except for the nanocapsule formulation containing both drugs [Capt(0.5)-Zn(25)-MLNC-Fur(0.45)]. For diastolic pressure, only Capt(0.5)-Zn(25)-MLNC-Fur(0.45) presented a significant di erence (p < 0.05) on the first day. On the fifth day, both Capt(0.5)-MLNC-Fur(0.45) and Capt(0.5)-Zn(25)-MLNC-Fur(0.45) had an e ect lasting up to 24 h. The analysis of early kidney damage marker showed a potential protection in renal function by Capt(0.5)-Zn(25)-MLNC-Fur(0.45). In conclusion, the formulation Capt(0.5)-Zn(25)-MLNC-Fur(0.45) proved to be suitable for hypertension treatment envisaging an important innovation. |
publishDate |
2020 |
dc.date.issued.fl_str_mv |
2020 |
dc.date.accessioned.fl_str_mv |
2021-11-04T04:23:52Z |
dc.type.driver.fl_str_mv |
Estrangeiro info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10183/231510 |
dc.identifier.issn.pt_BR.fl_str_mv |
1999-4923 |
dc.identifier.nrb.pt_BR.fl_str_mv |
001127987 |
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1999-4923 001127987 |
url |
http://hdl.handle.net/10183/231510 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
Pharmaceutics. Basel. Vol. 12, n. 1 (2020), 80, 23 p. |
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openAccess |
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