Comparative study of particle size distribution analysis by laser diffraction between dry and wet dispersion methods and scanning electron microscopy

Detalhes bibliográficos
Autor(a) principal: Sequeira, Sara Tomás
Data de Publicação: 2018
Tipo de documento: Dissertação
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10362/38119
Resumo: An Active pharmaceutical Ingredient (API) may assume several different physical forms such as dry powders, wet dispersions and semi-solid dispersions. Depending on the route of administration, the size of API particles may be considered a critical attribute, since this property may affect a variety of product characteristics, such as reactivity, stability, efficacy, texture, fluidity, viscosity, density among others. Fine API particles below ten micrometers in size, are required for pharmaceutical formulations administered by the pulmonary and ophthalmic routes. To achieve the desired particle size, several particle-engineering techniques may be employed. In this thesis, a variety of products (API’s & excipients) essentially intended for use in inhalation and ophthalmic formulations were characterized regarding particle size before and after being processed by particle engineering techniques. In order to evaluate the particle size distribution of the studied products, two laser diffraction techniques and an electron microscopy technique were used. The laser diffraction techniques used are based on the same theoretical principles however the mathematical algorithm used for data conversion and the particulate dispersion medium are different. For analysis by wet dispersion, the equipment used was Malvern Mastersizer Hydro 2000 S and Mastersizer 3000 Hydro MV. For the analysis by dry dispersion, the equipment used was Sympatec (comprising the units Helos, Rodos / M and Aspiros). Further characterization regarding particle size and morphology was carried out in a Phenom ProX Generation 5 microscope, a scanning electron microscope (SEM). During the course of this work, whenever possible, the above mentioned techniques were used and a comparison between them was done. Since these two laser diffraction techniques use different mathematical models for generating PSD data, it is expected that the PSD values reported are not exactly coincident. This means that every PS request should be always reported to a validated method.
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spelling Comparative study of particle size distribution analysis by laser diffraction between dry and wet dispersion methods and scanning electron microscopyAPIparticle engineeringPSDlaser diffraction (wet and dry dispersion)SEMDomínio/Área Científica::Engenharia e Tecnologia::Engenharia QuímicaAn Active pharmaceutical Ingredient (API) may assume several different physical forms such as dry powders, wet dispersions and semi-solid dispersions. Depending on the route of administration, the size of API particles may be considered a critical attribute, since this property may affect a variety of product characteristics, such as reactivity, stability, efficacy, texture, fluidity, viscosity, density among others. Fine API particles below ten micrometers in size, are required for pharmaceutical formulations administered by the pulmonary and ophthalmic routes. To achieve the desired particle size, several particle-engineering techniques may be employed. In this thesis, a variety of products (API’s & excipients) essentially intended for use in inhalation and ophthalmic formulations were characterized regarding particle size before and after being processed by particle engineering techniques. In order to evaluate the particle size distribution of the studied products, two laser diffraction techniques and an electron microscopy technique were used. The laser diffraction techniques used are based on the same theoretical principles however the mathematical algorithm used for data conversion and the particulate dispersion medium are different. For analysis by wet dispersion, the equipment used was Malvern Mastersizer Hydro 2000 S and Mastersizer 3000 Hydro MV. For the analysis by dry dispersion, the equipment used was Sympatec (comprising the units Helos, Rodos / M and Aspiros). Further characterization regarding particle size and morphology was carried out in a Phenom ProX Generation 5 microscope, a scanning electron microscope (SEM). During the course of this work, whenever possible, the above mentioned techniques were used and a comparison between them was done. Since these two laser diffraction techniques use different mathematical models for generating PSD data, it is expected that the PSD values reported are not exactly coincident. This means that every PS request should be always reported to a validated method.Silva, SérgioRicardo, AnaRUNSequeira, Sara Tomás2021-04-11T00:30:16Z2018-0520182018-05-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://hdl.handle.net/10362/38119enginfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T04:21:08Zoai:run.unl.pt:10362/38119Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:30:58.431247Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Comparative study of particle size distribution analysis by laser diffraction between dry and wet dispersion methods and scanning electron microscopy
title Comparative study of particle size distribution analysis by laser diffraction between dry and wet dispersion methods and scanning electron microscopy
spellingShingle Comparative study of particle size distribution analysis by laser diffraction between dry and wet dispersion methods and scanning electron microscopy
Sequeira, Sara Tomás
API
particle engineering
PSD
laser diffraction (wet and dry dispersion)
SEM
Domínio/Área Científica::Engenharia e Tecnologia::Engenharia Química
title_short Comparative study of particle size distribution analysis by laser diffraction between dry and wet dispersion methods and scanning electron microscopy
title_full Comparative study of particle size distribution analysis by laser diffraction between dry and wet dispersion methods and scanning electron microscopy
title_fullStr Comparative study of particle size distribution analysis by laser diffraction between dry and wet dispersion methods and scanning electron microscopy
title_full_unstemmed Comparative study of particle size distribution analysis by laser diffraction between dry and wet dispersion methods and scanning electron microscopy
title_sort Comparative study of particle size distribution analysis by laser diffraction between dry and wet dispersion methods and scanning electron microscopy
author Sequeira, Sara Tomás
author_facet Sequeira, Sara Tomás
author_role author
dc.contributor.none.fl_str_mv Silva, Sérgio
Ricardo, Ana
RUN
dc.contributor.author.fl_str_mv Sequeira, Sara Tomás
dc.subject.por.fl_str_mv API
particle engineering
PSD
laser diffraction (wet and dry dispersion)
SEM
Domínio/Área Científica::Engenharia e Tecnologia::Engenharia Química
topic API
particle engineering
PSD
laser diffraction (wet and dry dispersion)
SEM
Domínio/Área Científica::Engenharia e Tecnologia::Engenharia Química
description An Active pharmaceutical Ingredient (API) may assume several different physical forms such as dry powders, wet dispersions and semi-solid dispersions. Depending on the route of administration, the size of API particles may be considered a critical attribute, since this property may affect a variety of product characteristics, such as reactivity, stability, efficacy, texture, fluidity, viscosity, density among others. Fine API particles below ten micrometers in size, are required for pharmaceutical formulations administered by the pulmonary and ophthalmic routes. To achieve the desired particle size, several particle-engineering techniques may be employed. In this thesis, a variety of products (API’s & excipients) essentially intended for use in inhalation and ophthalmic formulations were characterized regarding particle size before and after being processed by particle engineering techniques. In order to evaluate the particle size distribution of the studied products, two laser diffraction techniques and an electron microscopy technique were used. The laser diffraction techniques used are based on the same theoretical principles however the mathematical algorithm used for data conversion and the particulate dispersion medium are different. For analysis by wet dispersion, the equipment used was Malvern Mastersizer Hydro 2000 S and Mastersizer 3000 Hydro MV. For the analysis by dry dispersion, the equipment used was Sympatec (comprising the units Helos, Rodos / M and Aspiros). Further characterization regarding particle size and morphology was carried out in a Phenom ProX Generation 5 microscope, a scanning electron microscope (SEM). During the course of this work, whenever possible, the above mentioned techniques were used and a comparison between them was done. Since these two laser diffraction techniques use different mathematical models for generating PSD data, it is expected that the PSD values reported are not exactly coincident. This means that every PS request should be always reported to a validated method.
publishDate 2018
dc.date.none.fl_str_mv 2018-05
2018
2018-05-01T00:00:00Z
2021-04-11T00:30:16Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10362/38119
url http://hdl.handle.net/10362/38119
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
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