Influence of polymer content on stabilizing milled amorphous salbutamol sulphate

The study investigates the influence of polyvinyl pyrrolidone (PVP) concentration on stabilizing the amorphous form of salbutamol sulphate (SS) before and after storage under ambient and elevated humidity conditions. Different mass ratios of SS and PVP (0–90 wt%) were co-milled using a planetary bal...

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Veröffentlicht in:International journal of pharmaceutics 2010-05, Vol.391 (1), p.125-136
Hauptverfasser: Balani, P.N., Wong, S.Y., Ng, W.K., Widjaja, E., Tan, R.B.H., Chan, S.Y.
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container_end_page 136
container_issue 1
container_start_page 125
container_title International journal of pharmaceutics
container_volume 391
creator Balani, P.N.
Wong, S.Y.
Ng, W.K.
Widjaja, E.
Tan, R.B.H.
Chan, S.Y.
description The study investigates the influence of polyvinyl pyrrolidone (PVP) concentration on stabilizing the amorphous form of salbutamol sulphate (SS) before and after storage under ambient and elevated humidity conditions. Different mass ratios of SS and PVP (0–90 wt%) were co-milled using a planetary ball mill. X-ray powder diffraction (XRPD), high sensitivity differential scanning calorimetry (HSDSC), dynamic vapor sorption (DVS), infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and Raman microscopy (RM) were used to analyze the stability of the co-milled mixtures against heat and humidity treatments as well as storage at different humidity conditions. Prior storage, DSC and DVS analyses revealed that re-crystallization of amorphous SS was suppressed above PVP content of 33 wt%. Probable hydrogen bond interaction between SS and PVP was found in FT-IR analysis. XRPD diffractograms and SEM analysis showed stability against re-crystallization was achieved in the co-milled mixtures with a minimum PVP content of 80 wt% after storage. Homogeneous distribution of SS and PVP from RM analysis showed fine clustering of SS and PVP, suggesting the formation of an amorphous dispersion at molecular level. The results provide insights on the application of thermal and humidity treatments, accelerated stability testing and investigations on drug–excipient interactions to predict the minimum ratio of an excipient for stabilizing the amorphous state of a milled API.
doi_str_mv 10.1016/j.ijpharm.2010.02.029
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Different mass ratios of SS and PVP (0–90 wt%) were co-milled using a planetary ball mill. X-ray powder diffraction (XRPD), high sensitivity differential scanning calorimetry (HSDSC), dynamic vapor sorption (DVS), infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and Raman microscopy (RM) were used to analyze the stability of the co-milled mixtures against heat and humidity treatments as well as storage at different humidity conditions. Prior storage, DSC and DVS analyses revealed that re-crystallization of amorphous SS was suppressed above PVP content of 33 wt%. Probable hydrogen bond interaction between SS and PVP was found in FT-IR analysis. XRPD diffractograms and SEM analysis showed stability against re-crystallization was achieved in the co-milled mixtures with a minimum PVP content of 80 wt% after storage. Homogeneous distribution of SS and PVP from RM analysis showed fine clustering of SS and PVP, suggesting the formation of an amorphous dispersion at molecular level. 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Different mass ratios of SS and PVP (0–90 wt%) were co-milled using a planetary ball mill. X-ray powder diffraction (XRPD), high sensitivity differential scanning calorimetry (HSDSC), dynamic vapor sorption (DVS), infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and Raman microscopy (RM) were used to analyze the stability of the co-milled mixtures against heat and humidity treatments as well as storage at different humidity conditions. Prior storage, DSC and DVS analyses revealed that re-crystallization of amorphous SS was suppressed above PVP content of 33 wt%. Probable hydrogen bond interaction between SS and PVP was found in FT-IR analysis. XRPD diffractograms and SEM analysis showed stability against re-crystallization was achieved in the co-milled mixtures with a minimum PVP content of 80 wt% after storage. Homogeneous distribution of SS and PVP from RM analysis showed fine clustering of SS and PVP, suggesting the formation of an amorphous dispersion at molecular level. The results provide insights on the application of thermal and humidity treatments, accelerated stability testing and investigations on drug–excipient interactions to predict the minimum ratio of an excipient for stabilizing the amorphous state of a milled API.</description><subject>Albuterol - chemistry</subject><subject>Biological and medical sciences</subject><subject>Co-milling</subject><subject>Crystallization - methods</subject><subject>Drug Compounding - instrumentation</subject><subject>Drug Compounding - methods</subject><subject>Drug Stability</subject><subject>Drug Storage</subject><subject>Excipients - chemistry</subject><subject>General pharmacology</subject><subject>Hot Temperature - adverse effects</subject><subject>Humidity - adverse effects</subject><subject>Medical sciences</subject><subject>Particle Size</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Polymers - chemistry</subject><subject>Polyvinyl pyrrolidone K30</subject><subject>Povidone - chemistry</subject><subject>Raman microscopy</subject><subject>Salbutamol sulphate</subject><subject>Stability</subject><subject>Surface Properties</subject><subject>X-ray powder diffraction</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1r3DAQhkVoSTZpf0KLLiUnb0aSLa1PpYR8QSA9JGchS-NGi2y5kh1If3217LY5BgakGZ6RXh5CvjBYM2DyYrv22-nZpGHNocyAl2qPyIptlKhEreQHsgKhNlXDlDghpzlvAUByJo7JCQfOmGJqRX7ejX1YcLRIY0-nGF4HTNTGccZxpnGkeTadD_6PH3_RwYeAjpohpuk5LplmE7plLn2geQklzoyfyMfehIyfD-cZebq-ery8re4fbu4uf9xXVrT1XNlNz1FZKVFKaRhztXNCNcy1rG-sLfe2txJtBxK4Amg5QGNa09WMdQ04cUbO9-9OKf5eMM968NliCGbEEk0rUQNvuOKFbPakTTHnhL2ekh9MetUM9M6l3uqDS71zqYGXasve18MPSzeg-7_1T14Bvh0Ak60JfTKj9fmN46oRku-473sOi48Xj0ln63fKnU9oZ-2ifyfKXynxlcs</recordid><startdate>20100531</startdate><enddate>20100531</enddate><creator>Balani, P.N.</creator><creator>Wong, S.Y.</creator><creator>Ng, W.K.</creator><creator>Widjaja, E.</creator><creator>Tan, R.B.H.</creator><creator>Chan, S.Y.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>20100531</creationdate><title>Influence of polymer content on stabilizing milled amorphous salbutamol sulphate</title><author>Balani, P.N. ; Wong, S.Y. ; Ng, W.K. ; Widjaja, E. ; Tan, R.B.H. ; Chan, S.Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c394t-c8f2e7c66e666a11d4dd3751d91f5ccd379fc6ecb060270092005a9ab411b50d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Albuterol - chemistry</topic><topic>Biological and medical sciences</topic><topic>Co-milling</topic><topic>Crystallization - methods</topic><topic>Drug Compounding - instrumentation</topic><topic>Drug Compounding - methods</topic><topic>Drug Stability</topic><topic>Drug Storage</topic><topic>Excipients - chemistry</topic><topic>General pharmacology</topic><topic>Hot Temperature - adverse effects</topic><topic>Humidity - adverse effects</topic><topic>Medical sciences</topic><topic>Particle Size</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Polymers - chemistry</topic><topic>Polyvinyl pyrrolidone K30</topic><topic>Povidone - chemistry</topic><topic>Raman microscopy</topic><topic>Salbutamol sulphate</topic><topic>Stability</topic><topic>Surface Properties</topic><topic>X-ray powder diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Balani, P.N.</creatorcontrib><creatorcontrib>Wong, S.Y.</creatorcontrib><creatorcontrib>Ng, W.K.</creatorcontrib><creatorcontrib>Widjaja, E.</creatorcontrib><creatorcontrib>Tan, R.B.H.</creatorcontrib><creatorcontrib>Chan, S.Y.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Balani, P.N.</au><au>Wong, S.Y.</au><au>Ng, W.K.</au><au>Widjaja, E.</au><au>Tan, R.B.H.</au><au>Chan, S.Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of polymer content on stabilizing milled amorphous salbutamol sulphate</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2010-05-31</date><risdate>2010</risdate><volume>391</volume><issue>1</issue><spage>125</spage><epage>136</epage><pages>125-136</pages><issn>0378-5173</issn><eissn>1873-3476</eissn><coden>IJPHDE</coden><abstract>The study investigates the influence of polyvinyl pyrrolidone (PVP) concentration on stabilizing the amorphous form of salbutamol sulphate (SS) before and after storage under ambient and elevated humidity conditions. 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Homogeneous distribution of SS and PVP from RM analysis showed fine clustering of SS and PVP, suggesting the formation of an amorphous dispersion at molecular level. The results provide insights on the application of thermal and humidity treatments, accelerated stability testing and investigations on drug–excipient interactions to predict the minimum ratio of an excipient for stabilizing the amorphous state of a milled API.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>20211717</pmid><doi>10.1016/j.ijpharm.2010.02.029</doi><tpages>12</tpages></addata></record>
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subjects Albuterol - chemistry
Biological and medical sciences
Co-milling
Crystallization - methods
Drug Compounding - instrumentation
Drug Compounding - methods
Drug Stability
Drug Storage
Excipients - chemistry
General pharmacology
Hot Temperature - adverse effects
Humidity - adverse effects
Medical sciences
Particle Size
Pharmaceutical technology. Pharmaceutical industry
Pharmacology. Drug treatments
Polymers - chemistry
Polyvinyl pyrrolidone K30
Povidone - chemistry
Raman microscopy
Salbutamol sulphate
Stability
Surface Properties
X-ray powder diffraction
title Influence of polymer content on stabilizing milled amorphous salbutamol sulphate
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