Oral treatment of spontaneously hypertensive rats with captopril-surface functionalized furosemide-loaded multi-wall lipid-core nanocapsules

Detalhes bibliográficos
Autor(a) principal: Michalowski, Cecilia Bohns
Data de Publicação: 2020
Outros Autores: 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
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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spelling 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 de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar: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
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dc.identifier.nrb.pt_BR.fl_str_mv 001127987
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dc.relation.ispartof.pt_BR.fl_str_mv Pharmaceutics. Basel. Vol. 12, n. 1 (2020), 80, 23 p.
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