Cargando…

Preparation, characterization, and pharmacodynamics of insulin-loaded fumaryl diketopiperazine microparticle dry powder inhalation

Purpose: With the increase of population aging and the proportion of overweight and obese, a growing number of people are suffering from diabetes. Insulin (INS) as the most widely used hypoglycemic agent was always chosen as the most effective treatment method of diabetes. In this study, fumaryl dik...

Descripción completa

Detalles Bibliográficos
Autores principales: Xia, Yun, Su, Yipeng, Wang, Qiyue, Yang, Chen, Tang, Baoqiang, Zhang, Yue, Tu, Jiasheng, Shen, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609328/
https://www.ncbi.nlm.nih.gov/pubmed/31257946
http://dx.doi.org/10.1080/10717544.2019.1631408
_version_ 1783432293306597376
author Xia, Yun
Su, Yipeng
Wang, Qiyue
Yang, Chen
Tang, Baoqiang
Zhang, Yue
Tu, Jiasheng
Shen, Yan
author_facet Xia, Yun
Su, Yipeng
Wang, Qiyue
Yang, Chen
Tang, Baoqiang
Zhang, Yue
Tu, Jiasheng
Shen, Yan
author_sort Xia, Yun
collection PubMed
description Purpose: With the increase of population aging and the proportion of overweight and obese, a growing number of people are suffering from diabetes. Insulin (INS) as the most widely used hypoglycemic agent was always chosen as the most effective treatment method of diabetes. In this study, fumaryl diketopiperazine (FDKP) was used as a carrier for the pulmonary delivery of insulin. Patients and methods: The INS-loaded FDKP microspheres (INS@FDKP-MPs) were prepared by spray drying and physicochemical properties (drug loading, particle size, flowability, moisture content, morphology, and crystalline state) were further investigated. Pharmacodynamics was investigated on diabetic model rats administrated by intratracheal insufflation. Results: The INS-loaded FDKP microspheres show satisfied flowability and in vitro deposition with FPF 50.2% and MMAD 3.45 ± 0.13 μm, and the blood glucose level was significantly decreased. Moreover, no inflammatory reaction was observed during the safety study. Conclusion: To sum up, the aim was to develop a non-injection system for insulin, INS@FDKP-MPs powder inhalation with high dose, low toxicity, and good lung deposition inhalation could rapidly decrease the blood glucose level without immune stimulation, which shows remarkably potential on diabetes treatment by pulmonary delivery route.
format Online
Article
Text
id pubmed-6609328
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-66093282019-07-12 Preparation, characterization, and pharmacodynamics of insulin-loaded fumaryl diketopiperazine microparticle dry powder inhalation Xia, Yun Su, Yipeng Wang, Qiyue Yang, Chen Tang, Baoqiang Zhang, Yue Tu, Jiasheng Shen, Yan Drug Deliv Research Article Purpose: With the increase of population aging and the proportion of overweight and obese, a growing number of people are suffering from diabetes. Insulin (INS) as the most widely used hypoglycemic agent was always chosen as the most effective treatment method of diabetes. In this study, fumaryl diketopiperazine (FDKP) was used as a carrier for the pulmonary delivery of insulin. Patients and methods: The INS-loaded FDKP microspheres (INS@FDKP-MPs) were prepared by spray drying and physicochemical properties (drug loading, particle size, flowability, moisture content, morphology, and crystalline state) were further investigated. Pharmacodynamics was investigated on diabetic model rats administrated by intratracheal insufflation. Results: The INS-loaded FDKP microspheres show satisfied flowability and in vitro deposition with FPF 50.2% and MMAD 3.45 ± 0.13 μm, and the blood glucose level was significantly decreased. Moreover, no inflammatory reaction was observed during the safety study. Conclusion: To sum up, the aim was to develop a non-injection system for insulin, INS@FDKP-MPs powder inhalation with high dose, low toxicity, and good lung deposition inhalation could rapidly decrease the blood glucose level without immune stimulation, which shows remarkably potential on diabetes treatment by pulmonary delivery route. Taylor & Francis 2019-07-01 /pmc/articles/PMC6609328/ /pubmed/31257946 http://dx.doi.org/10.1080/10717544.2019.1631408 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Xia, Yun
Su, Yipeng
Wang, Qiyue
Yang, Chen
Tang, Baoqiang
Zhang, Yue
Tu, Jiasheng
Shen, Yan
Preparation, characterization, and pharmacodynamics of insulin-loaded fumaryl diketopiperazine microparticle dry powder inhalation
title Preparation, characterization, and pharmacodynamics of insulin-loaded fumaryl diketopiperazine microparticle dry powder inhalation
title_full Preparation, characterization, and pharmacodynamics of insulin-loaded fumaryl diketopiperazine microparticle dry powder inhalation
title_fullStr Preparation, characterization, and pharmacodynamics of insulin-loaded fumaryl diketopiperazine microparticle dry powder inhalation
title_full_unstemmed Preparation, characterization, and pharmacodynamics of insulin-loaded fumaryl diketopiperazine microparticle dry powder inhalation
title_short Preparation, characterization, and pharmacodynamics of insulin-loaded fumaryl diketopiperazine microparticle dry powder inhalation
title_sort preparation, characterization, and pharmacodynamics of insulin-loaded fumaryl diketopiperazine microparticle dry powder inhalation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609328/
https://www.ncbi.nlm.nih.gov/pubmed/31257946
http://dx.doi.org/10.1080/10717544.2019.1631408
work_keys_str_mv AT xiayun preparationcharacterizationandpharmacodynamicsofinsulinloadedfumaryldiketopiperazinemicroparticledrypowderinhalation
AT suyipeng preparationcharacterizationandpharmacodynamicsofinsulinloadedfumaryldiketopiperazinemicroparticledrypowderinhalation
AT wangqiyue preparationcharacterizationandpharmacodynamicsofinsulinloadedfumaryldiketopiperazinemicroparticledrypowderinhalation
AT yangchen preparationcharacterizationandpharmacodynamicsofinsulinloadedfumaryldiketopiperazinemicroparticledrypowderinhalation
AT tangbaoqiang preparationcharacterizationandpharmacodynamicsofinsulinloadedfumaryldiketopiperazinemicroparticledrypowderinhalation
AT zhangyue preparationcharacterizationandpharmacodynamicsofinsulinloadedfumaryldiketopiperazinemicroparticledrypowderinhalation
AT tujiasheng preparationcharacterizationandpharmacodynamicsofinsulinloadedfumaryldiketopiperazinemicroparticledrypowderinhalation
AT shenyan preparationcharacterizationandpharmacodynamicsofinsulinloadedfumaryldiketopiperazinemicroparticledrypowderinhalation