H. B. Samal, Lipsa Samal, Annada Kar, Itishree Jogamaya Das, Bishal Sarkar, Arijit Mondal, Suddhasattya Dey
{"title":"Formulation and Evaluation of Aprepitant Nanosuspension by Nano Precipitation Techniques","authors":"H. B. Samal, Lipsa Samal, Annada Kar, Itishree Jogamaya Das, Bishal Sarkar, Arijit Mondal, Suddhasattya Dey","doi":"10.2174/0124681873299074240307093319","DOIUrl":null,"url":null,"abstract":"\n\nThe majority of new chemical substances generated by the drug development\nprocess are poorly water-soluble or lipophilic. Formulation of a poorly water-soluble substance\nis a difficult task for the pharmaceutical industry. It is widely acknowledged that using nanosuspension\nin drug administration enhances the drug’s solubility, dissolution, and ultimately bioavailability.\nThis study aimed to examine the particle sizes of nanosuspensions made by nanoprecipitation\ntechniques and improve their effectiveness.\n\n\n\nAprepitant’s nanosuspension has been produced by nanoprecipitation techniques. The\nparticle size, polydispersity index, along zeta potential of the produced nanosuspensions were measured.\nThe optimized nanosuspension has been investigated further for solubility, dissolution, surface\nmorphology, FT-IR, DSC as well as stability studies.\n\n\n\nThe majority of new chemical substances generated by the drug development process are poorly water soluble or lipophilic. Formulation of a poorly water-soluble substance is a difficult task for the pharmaceutical industry. It is widely acknowledged that using nanosuspension in drug administration enhances the drug’s solubility, dissolution, and ultimately bioavailability. This study aimed to examine the particle sizes of nanosuspensions made by nano precipitation techniques and improve its effectiveness.\n\n\n\nThe combination of tween 80 and poloxamer 188 as stabilizer resulted in the preparation\nof an optimized nanosuspension (F9) with a particle size of 738 nm, polydispersity index 0.236,\nzeta potential -15.1 mV and an improved solubility and dissolution profile compared to pure\ndrugs. Positive performance improvement was observed in the solubility and dissolution studies.\nThe crystallinity changed upon nanosizing, as demonstrated by the SEM, FT-IR and DSC analysis.\n\n\n\nAprepitant’s nanosuspension has been produced by nano precipitation techniques. The particle size, polydispersity index along with zeta potential of the produced nanosuspensions were measured. The optimized nanosuspension has been investigated further for solubility, dissolution, surface morphology, FT-IR, DSC as well as stability studies.\n\n\n\nThe nanoprecipitation method was effective in producing a stable Aprepitant nanosuspension\nwith improved solubility and dissolution rate.\n","PeriodicalId":10818,"journal":{"name":"Current Nanomedicine","volume":" 23","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Nanomedicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0124681873299074240307093319","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
The majority of new chemical substances generated by the drug development
process are poorly water-soluble or lipophilic. Formulation of a poorly water-soluble substance
is a difficult task for the pharmaceutical industry. It is widely acknowledged that using nanosuspension
in drug administration enhances the drug’s solubility, dissolution, and ultimately bioavailability.
This study aimed to examine the particle sizes of nanosuspensions made by nanoprecipitation
techniques and improve their effectiveness.
Aprepitant’s nanosuspension has been produced by nanoprecipitation techniques. The
particle size, polydispersity index, along zeta potential of the produced nanosuspensions were measured.
The optimized nanosuspension has been investigated further for solubility, dissolution, surface
morphology, FT-IR, DSC as well as stability studies.
The majority of new chemical substances generated by the drug development process are poorly water soluble or lipophilic. Formulation of a poorly water-soluble substance is a difficult task for the pharmaceutical industry. It is widely acknowledged that using nanosuspension in drug administration enhances the drug’s solubility, dissolution, and ultimately bioavailability. This study aimed to examine the particle sizes of nanosuspensions made by nano precipitation techniques and improve its effectiveness.
The combination of tween 80 and poloxamer 188 as stabilizer resulted in the preparation
of an optimized nanosuspension (F9) with a particle size of 738 nm, polydispersity index 0.236,
zeta potential -15.1 mV and an improved solubility and dissolution profile compared to pure
drugs. Positive performance improvement was observed in the solubility and dissolution studies.
The crystallinity changed upon nanosizing, as demonstrated by the SEM, FT-IR and DSC analysis.
Aprepitant’s nanosuspension has been produced by nano precipitation techniques. The particle size, polydispersity index along with zeta potential of the produced nanosuspensions were measured. The optimized nanosuspension has been investigated further for solubility, dissolution, surface morphology, FT-IR, DSC as well as stability studies.
The nanoprecipitation method was effective in producing a stable Aprepitant nanosuspension
with improved solubility and dissolution rate.