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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 |
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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 |
format | article |
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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><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 & 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</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 & dosage</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Antibacterial agents</subject><subject>Antibiotics</subject><subject>Azithromycin</subject><subject>Azithromycin - administration & 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 & 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 & dosage</subject><subject>Powders - chemistry</subject><subject>Research Paper</subject><subject>Respiration</subject><subject>Solubility</subject><subject>Spray drying</subject><subject>Surface Properties</subject><issn>0724-8741</issn><issn>1573-904X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1ksFu1DAQhi0EokvhAbggS1x6cfHY3sS5IK22FCpVAqkUcbMcx9l1ldiLnUDLy_CqOKQsLQL5YHnmn280nh-h50CPgdLyVQKg1ZJQkIQtWUmuH6AFLEtOKio-P0QLWjJBZCngAD1J6YpSKqESj9EBp4IWTMIC_bj0jY1p0L5xfoOHrcVn_U6bIeHQ4osxttpYvA79LiQ3uOBz3M8yTz65IQZ84lIK3TglccbglY0hB9x3_SuUMetALnZR35CT6Gyzp1n8IXzL3fFpiP3Y6RnfhpjZWz2_n6JHre6SfXZ7H6LL0zcf1-_I-fu3Z-vVOTEF5QNhDBqmrWksN42pqKwZazWAKGVBy6UoBas5q2RVM1uDlkUjNYWirMHUNbTAD9Hrmbsb6942xvoh6k7tout1vFFBO3U_491WbcJXVXBGuWAZcHQLiOHLaNOgepeM7TrtbRiTYsCBcQ6CZ-nLv6RXYYw-jzepaCEFyDuqje6scr4Nua-ZoGqV98qAAkxtj_-hyqexvTPB29bl-L0CmAtM3lKKtt3PCFRNrlKzq1R2lZpcpa5zzYu7n7Ov-G2jLGCzIOWU39j4Z6L_U38CswvaQQ</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Mangal, Sharad</creator><creator>Xu, Rongkun</creator><creator>Park, Heejun</creator><creator>Zemlyanov, Dmitry</creator><creator>Shetty, Nivedita</creator><creator>Lin, Yu-Wei</creator><creator>Morton, David</creator><creator>Chan, Hak-Kim</creator><creator>Li, Jian</creator><creator>Zhou, Qi Tony</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1438-6990</orcidid></search><sort><creationdate>20190101</creationdate><title>Understanding the Impacts of Surface Compositions on the In-Vitro Dissolution and Aerosolization of Co-Spray-Dried Composite Powder Formulations for Inhalation</title><author>Mangal, Sharad ; Xu, Rongkun ; Park, Heejun ; Zemlyanov, Dmitry ; Shetty, Nivedita ; Lin, Yu-Wei ; Morton, David ; Chan, Hak-Kim ; Li, Jian ; Zhou, Qi Tony</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c603t-221d2aecde3cdc908b22fa1147860754742b32989b2eb1a86d8a0167b1cbb1f13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Administration, Inhalation</topic><topic>Aerosols - chemistry</topic><topic>Anti-Bacterial Agents - administration & dosage</topic><topic>Anti-Bacterial Agents - chemistry</topic><topic>Antibacterial agents</topic><topic>Antibiotics</topic><topic>Azithromycin</topic><topic>Azithromycin - administration & dosage</topic><topic>Azithromycin - chemistry</topic><topic>Biochemistry</topic><topic>Biofilms</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedical Engineering and Bioengineering</topic><topic>Biomedicine</topic><topic>Chemistry, Pharmaceutical</topic><topic>Chronic obstructive pulmonary disease</topic><topic>Colistin</topic><topic>Colistin - administration & 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 & 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 & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mangal, Sharad</au><au>Xu, Rongkun</au><au>Park, Heejun</au><au>Zemlyanov, Dmitry</au><au>Shetty, Nivedita</au><au>Lin, Yu-Wei</au><au>Morton, David</au><au>Chan, Hak-Kim</au><au>Li, Jian</au><au>Zhou, Qi Tony</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Understanding the Impacts of Surface Compositions on the In-Vitro Dissolution and Aerosolization of Co-Spray-Dried Composite Powder Formulations for Inhalation</atitle><jtitle>Pharmaceutical research</jtitle><stitle>Pharm Res</stitle><addtitle>Pharm Res</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>36</volume><issue>1</issue><spage>6</spage><epage>15</epage><pages>6-15</pages><artnum>6</artnum><issn>0724-8741</issn><eissn>1573-904X</eissn><abstract>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.</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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source | Springer Nature |
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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