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Understanding the Impacts of Surface Compositions on the In-Vitro Dissolution and Aerosolization of Co-Spray-Dried Composite Powder Formulations for Inhalation

Purpose Dissolution behavior of dry powder inhaler (DPI) antibiotic formulations in the airways may affect their efficacy especially for poorly-soluble antibiotics such as azithromycin. The main objective of this study was to understand the effects of surface composition on the dissolution of spray...

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Published in:Pharmaceutical research 2019-01, Vol.36 (1), p.6-15, Article 6
Main Authors: Mangal, Sharad, Xu, Rongkun, Park, Heejun, Zemlyanov, Dmitry, Shetty, Nivedita, Lin, Yu-Wei, Morton, David, Chan, Hak-Kim, Li, Jian, Zhou, Qi Tony
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cited_by cdi_FETCH-LOGICAL-c603t-221d2aecde3cdc908b22fa1147860754742b32989b2eb1a86d8a0167b1cbb1f13
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container_title Pharmaceutical research
container_volume 36
creator Mangal, Sharad
Xu, Rongkun
Park, Heejun
Zemlyanov, Dmitry
Shetty, Nivedita
Lin, Yu-Wei
Morton, David
Chan, Hak-Kim
Li, Jian
Zhou, Qi Tony
description Purpose Dissolution behavior of dry powder inhaler (DPI) antibiotic formulations in the airways may affect their efficacy especially for poorly-soluble antibiotics such as azithromycin. The main objective of this study was to understand the effects of surface composition on the dissolution of spray dried azithromycin powders by itself and in combination with colistin. Methods Composite formulations of azithromycin (a poorly water-soluble molecule) and colistin (a water-soluble molecule) were produced by spray drying. The resultant formulations were characterized for particle size, morphology, surface composition, solid-state properties, solubility and dissolution. Results The results demonstrate that surfaces composition has critical impacts on the dissolution of composite formulations. Colistin was shown to increase the solubility of azithromycin. For composite formulations with no surface colistin, azithromycin released at a similar dissolution rate as the spray-dried azithromycin alone. An increase in surface colistin concentration was shown to accelerate the dissolution of azithromycin. The dissolution of colistin from the composite formulations was significantly slower than the spray-dried pure colistin. In addition, FTIR spectrum showed intermolecular interactions between azithromycin and colistin in the composite formulations, which could contribute to the enhanced solubility and dissolution of azithromycin. Conclusions Our study provides fundamental understanding of the effects of surface concentration of colistin on azithromycin dissolution of co-spray-dried composite powder formulations.
doi_str_mv 10.1007/s11095-018-2527-x
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The main objective of this study was to understand the effects of surface composition on the dissolution of spray dried azithromycin powders by itself and in combination with colistin. Methods Composite formulations of azithromycin (a poorly water-soluble molecule) and colistin (a water-soluble molecule) were produced by spray drying. The resultant formulations were characterized for particle size, morphology, surface composition, solid-state properties, solubility and dissolution. Results The results demonstrate that surfaces composition has critical impacts on the dissolution of composite formulations. Colistin was shown to increase the solubility of azithromycin. For composite formulations with no surface colistin, azithromycin released at a similar dissolution rate as the spray-dried azithromycin alone. An increase in surface colistin concentration was shown to accelerate the dissolution of azithromycin. The dissolution of colistin from the composite formulations was significantly slower than the spray-dried pure colistin. In addition, FTIR spectrum showed intermolecular interactions between azithromycin and colistin in the composite formulations, which could contribute to the enhanced solubility and dissolution of azithromycin. Conclusions Our study provides fundamental understanding of the effects of surface concentration of colistin on azithromycin dissolution of co-spray-dried composite powder formulations.</description><identifier>ISSN: 0724-8741</identifier><identifier>EISSN: 1573-904X</identifier><identifier>DOI: 10.1007/s11095-018-2527-x</identifier><identifier>PMID: 30406281</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Administration, Inhalation ; Aerosols - chemistry ; Anti-Bacterial Agents - administration &amp; dosage ; Anti-Bacterial Agents - chemistry ; Antibacterial agents ; Antibiotics ; Azithromycin ; Azithromycin - administration &amp; dosage ; Azithromycin - chemistry ; Biochemistry ; Biofilms ; Biomedical and Life Sciences ; Biomedical Engineering and Bioengineering ; Biomedicine ; Chemistry, Pharmaceutical ; Chronic obstructive pulmonary disease ; Colistin ; Colistin - administration &amp; dosage ; Colistin - chemistry ; Dissolution ; Drug Compounding - methods ; Drug delivery systems ; Drugs ; Dry Powder Inhalers ; Drying ; Formulations ; Humans ; Infections ; Inhalation ; Inhalers ; Lungs ; Medical Law ; Morphology ; Particle Size ; Pharmacology/Toxicology ; Pharmacy ; Powder ; Powders - administration &amp; dosage ; Powders - chemistry ; Research Paper ; Respiration ; Solubility ; Spray drying ; Surface Properties</subject><ispartof>Pharmaceutical research, 2019-01, Vol.36 (1), p.6-15, Article 6</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2018</rights><rights>COPYRIGHT 2019 Springer</rights><rights>Pharmaceutical Research is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c603t-221d2aecde3cdc908b22fa1147860754742b32989b2eb1a86d8a0167b1cbb1f13</citedby><cites>FETCH-LOGICAL-c603t-221d2aecde3cdc908b22fa1147860754742b32989b2eb1a86d8a0167b1cbb1f13</cites><orcidid>0000-0002-1438-6990</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30406281$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mangal, Sharad</creatorcontrib><creatorcontrib>Xu, Rongkun</creatorcontrib><creatorcontrib>Park, Heejun</creatorcontrib><creatorcontrib>Zemlyanov, Dmitry</creatorcontrib><creatorcontrib>Shetty, Nivedita</creatorcontrib><creatorcontrib>Lin, Yu-Wei</creatorcontrib><creatorcontrib>Morton, David</creatorcontrib><creatorcontrib>Chan, Hak-Kim</creatorcontrib><creatorcontrib>Li, Jian</creatorcontrib><creatorcontrib>Zhou, Qi Tony</creatorcontrib><title>Understanding the Impacts of Surface Compositions on the In-Vitro Dissolution and Aerosolization of Co-Spray-Dried Composite Powder Formulations for Inhalation</title><title>Pharmaceutical research</title><addtitle>Pharm Res</addtitle><addtitle>Pharm Res</addtitle><description>Purpose Dissolution behavior of dry powder inhaler (DPI) antibiotic formulations in the airways may affect their efficacy especially for poorly-soluble antibiotics such as azithromycin. The main objective of this study was to understand the effects of surface composition on the dissolution of spray dried azithromycin powders by itself and in combination with colistin. Methods Composite formulations of azithromycin (a poorly water-soluble molecule) and colistin (a water-soluble molecule) were produced by spray drying. The resultant formulations were characterized for particle size, morphology, surface composition, solid-state properties, solubility and dissolution. Results The results demonstrate that surfaces composition has critical impacts on the dissolution of composite formulations. Colistin was shown to increase the solubility of azithromycin. For composite formulations with no surface colistin, azithromycin released at a similar dissolution rate as the spray-dried azithromycin alone. An increase in surface colistin concentration was shown to accelerate the dissolution of azithromycin. The dissolution of colistin from the composite formulations was significantly slower than the spray-dried pure colistin. In addition, FTIR spectrum showed intermolecular interactions between azithromycin and colistin in the composite formulations, which could contribute to the enhanced solubility and dissolution of azithromycin. Conclusions Our study provides fundamental understanding of the effects of surface concentration of colistin on azithromycin dissolution of co-spray-dried composite powder formulations.</description><subject>Administration, Inhalation</subject><subject>Aerosols - chemistry</subject><subject>Anti-Bacterial Agents - administration &amp; dosage</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Antibacterial agents</subject><subject>Antibiotics</subject><subject>Azithromycin</subject><subject>Azithromycin - administration &amp; dosage</subject><subject>Azithromycin - chemistry</subject><subject>Biochemistry</subject><subject>Biofilms</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering and Bioengineering</subject><subject>Biomedicine</subject><subject>Chemistry, Pharmaceutical</subject><subject>Chronic obstructive pulmonary disease</subject><subject>Colistin</subject><subject>Colistin - administration &amp; dosage</subject><subject>Colistin - chemistry</subject><subject>Dissolution</subject><subject>Drug Compounding - methods</subject><subject>Drug delivery systems</subject><subject>Drugs</subject><subject>Dry Powder Inhalers</subject><subject>Drying</subject><subject>Formulations</subject><subject>Humans</subject><subject>Infections</subject><subject>Inhalation</subject><subject>Inhalers</subject><subject>Lungs</subject><subject>Medical Law</subject><subject>Morphology</subject><subject>Particle Size</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Powder</subject><subject>Powders - administration &amp; 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dosage</topic><topic>Colistin - chemistry</topic><topic>Dissolution</topic><topic>Drug Compounding - methods</topic><topic>Drug delivery systems</topic><topic>Drugs</topic><topic>Dry Powder Inhalers</topic><topic>Drying</topic><topic>Formulations</topic><topic>Humans</topic><topic>Infections</topic><topic>Inhalation</topic><topic>Inhalers</topic><topic>Lungs</topic><topic>Medical Law</topic><topic>Morphology</topic><topic>Particle Size</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>Powder</topic><topic>Powders - administration &amp; dosage</topic><topic>Powders - chemistry</topic><topic>Research Paper</topic><topic>Respiration</topic><topic>Solubility</topic><topic>Spray drying</topic><topic>Surface Properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mangal, Sharad</creatorcontrib><creatorcontrib>Xu, Rongkun</creatorcontrib><creatorcontrib>Park, Heejun</creatorcontrib><creatorcontrib>Zemlyanov, Dmitry</creatorcontrib><creatorcontrib>Shetty, Nivedita</creatorcontrib><creatorcontrib>Lin, Yu-Wei</creatorcontrib><creatorcontrib>Morton, David</creatorcontrib><creatorcontrib>Chan, Hak-Kim</creatorcontrib><creatorcontrib>Li, Jian</creatorcontrib><creatorcontrib>Zhou, Qi Tony</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health &amp; 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The main objective of this study was to understand the effects of surface composition on the dissolution of spray dried azithromycin powders by itself and in combination with colistin. Methods Composite formulations of azithromycin (a poorly water-soluble molecule) and colistin (a water-soluble molecule) were produced by spray drying. The resultant formulations were characterized for particle size, morphology, surface composition, solid-state properties, solubility and dissolution. Results The results demonstrate that surfaces composition has critical impacts on the dissolution of composite formulations. Colistin was shown to increase the solubility of azithromycin. For composite formulations with no surface colistin, azithromycin released at a similar dissolution rate as the spray-dried azithromycin alone. An increase in surface colistin concentration was shown to accelerate the dissolution of azithromycin. The dissolution of colistin from the composite formulations was significantly slower than the spray-dried pure colistin. In addition, FTIR spectrum showed intermolecular interactions between azithromycin and colistin in the composite formulations, which could contribute to the enhanced solubility and dissolution of azithromycin. Conclusions Our study provides fundamental understanding of the effects of surface concentration of colistin on azithromycin dissolution of co-spray-dried composite powder formulations.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>30406281</pmid><doi>10.1007/s11095-018-2527-x</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-1438-6990</orcidid><oa>free_for_read</oa></addata></record>
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subjects Administration, Inhalation
Aerosols - chemistry
Anti-Bacterial Agents - administration & dosage
Anti-Bacterial Agents - chemistry
Antibacterial agents
Antibiotics
Azithromycin
Azithromycin - administration & dosage
Azithromycin - chemistry
Biochemistry
Biofilms
Biomedical and Life Sciences
Biomedical Engineering and Bioengineering
Biomedicine
Chemistry, Pharmaceutical
Chronic obstructive pulmonary disease
Colistin
Colistin - administration & dosage
Colistin - chemistry
Dissolution
Drug Compounding - methods
Drug delivery systems
Drugs
Dry Powder Inhalers
Drying
Formulations
Humans
Infections
Inhalation
Inhalers
Lungs
Medical Law
Morphology
Particle Size
Pharmacology/Toxicology
Pharmacy
Powder
Powders - administration & dosage
Powders - chemistry
Research Paper
Respiration
Solubility
Spray drying
Surface Properties
title Understanding the Impacts of Surface Compositions on the In-Vitro Dissolution and Aerosolization of Co-Spray-Dried Composite Powder Formulations for Inhalation
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