Application of perfluoropolyether elastomers in microfluidic drug metabolism assays

[Display omitted] •Perfluoropolyether elastomers are useful in the fabrication of microfluidic devices.•Perfluoropolyether elastomers exhibit high biocompatibility and chemical repellency.•Hansen solubility parameters predict drug sorption into device materials.•Microfluidic flow improves cellular f...

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Veröffentlicht in:International journal of pharmaceutics 2022-11, Vol.627, p.122253-122253, Article 122253
Hauptverfasser: Wang, Mengyang, Tsuda, Masahiro, Deguchi, Sayaka, Higuchi, Yuriko, So, Kanako, Torisawa, Yu-suke, Takayama, Kazuo, Yamashita, Fumiyoshi
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container_title International journal of pharmaceutics
container_volume 627
creator Wang, Mengyang
Tsuda, Masahiro
Deguchi, Sayaka
Higuchi, Yuriko
So, Kanako
Torisawa, Yu-suke
Takayama, Kazuo
Yamashita, Fumiyoshi
description [Display omitted] •Perfluoropolyether elastomers are useful in the fabrication of microfluidic devices.•Perfluoropolyether elastomers exhibit high biocompatibility and chemical repellency.•Hansen solubility parameters predict drug sorption into device materials.•Microfluidic flow improves cellular function and metabolic activity of cultured hepatocytes. Recently, increasing attention has been paid to liver-on-a-chip models for both pharmacokinetics and toxicity (ADMET) screenings. Although polydimethylsiloxane (PDMS) is the most popular material for the fabrication of microfluidic devices, its extensive sorption of hydrophobic drugs limits its applications. Therefore, we investigated a chemically repellent material, perfluoropolyether (PFPE) elastomer, as an alternative to PDMS. Primary rat hepatocytes cultured in the PFPE microfluidic device were polygonal or cuboidal in shape and had one or two prominent nuclei, as when cultured in 96-well plates. When hepatocytes were cultured in the PFPE microfluidic device and exposed to dynamic flow, the production of albumin and urea increased 3.94- and 1.72-fold, respectively, compared with no dynamic flow. Exposure to dynamic flow did not result in obvious changes in the expression of cytochrome P450, but increased the metabolic activity of hepatocytes compared to under static conditions. PFPE devices did not absorb midazolam, which was extensively absorbed by PDMS devices. However, the sorption of bufuralol could not be avoided even with PFPE devices. Solvent swelling experiments highlighted much better chemical repellency with PFPE than with PDMS. Hansen solubility parameters and sphere radius were estimated from the solvent swelling experiments. The relative energy distance (RED) of bufuralol to PFPE was much smaller than that of other three drugs tested, reasonably explaining the high sorption of bufuralol to PFPE. Although sorption into PFPE cannot be completely avoided, PFPE microfluidic devices may provide a better performance in ADMET evaluation than PDMS.
doi_str_mv 10.1016/j.ijpharm.2022.122253
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Recently, increasing attention has been paid to liver-on-a-chip models for both pharmacokinetics and toxicity (ADMET) screenings. Although polydimethylsiloxane (PDMS) is the most popular material for the fabrication of microfluidic devices, its extensive sorption of hydrophobic drugs limits its applications. Therefore, we investigated a chemically repellent material, perfluoropolyether (PFPE) elastomer, as an alternative to PDMS. Primary rat hepatocytes cultured in the PFPE microfluidic device were polygonal or cuboidal in shape and had one or two prominent nuclei, as when cultured in 96-well plates. When hepatocytes were cultured in the PFPE microfluidic device and exposed to dynamic flow, the production of albumin and urea increased 3.94- and 1.72-fold, respectively, compared with no dynamic flow. Exposure to dynamic flow did not result in obvious changes in the expression of cytochrome P450, but increased the metabolic activity of hepatocytes compared to under static conditions. PFPE devices did not absorb midazolam, which was extensively absorbed by PDMS devices. However, the sorption of bufuralol could not be avoided even with PFPE devices. Solvent swelling experiments highlighted much better chemical repellency with PFPE than with PDMS. Hansen solubility parameters and sphere radius were estimated from the solvent swelling experiments. The relative energy distance (RED) of bufuralol to PFPE was much smaller than that of other three drugs tested, reasonably explaining the high sorption of bufuralol to PFPE. 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Recently, increasing attention has been paid to liver-on-a-chip models for both pharmacokinetics and toxicity (ADMET) screenings. Although polydimethylsiloxane (PDMS) is the most popular material for the fabrication of microfluidic devices, its extensive sorption of hydrophobic drugs limits its applications. Therefore, we investigated a chemically repellent material, perfluoropolyether (PFPE) elastomer, as an alternative to PDMS. Primary rat hepatocytes cultured in the PFPE microfluidic device were polygonal or cuboidal in shape and had one or two prominent nuclei, as when cultured in 96-well plates. When hepatocytes were cultured in the PFPE microfluidic device and exposed to dynamic flow, the production of albumin and urea increased 3.94- and 1.72-fold, respectively, compared with no dynamic flow. Exposure to dynamic flow did not result in obvious changes in the expression of cytochrome P450, but increased the metabolic activity of hepatocytes compared to under static conditions. PFPE devices did not absorb midazolam, which was extensively absorbed by PDMS devices. However, the sorption of bufuralol could not be avoided even with PFPE devices. Solvent swelling experiments highlighted much better chemical repellency with PFPE than with PDMS. Hansen solubility parameters and sphere radius were estimated from the solvent swelling experiments. The relative energy distance (RED) of bufuralol to PFPE was much smaller than that of other three drugs tested, reasonably explaining the high sorption of bufuralol to PFPE. Although sorption into PFPE cannot be completely avoided, PFPE microfluidic devices may provide a better performance in ADMET evaluation than PDMS.</description><subject>Chemical repellency</subject><subject>Hansen solubility parameters</subject><subject>Liver metabolism</subject><subject>Microfluidic device</subject><subject>Perfluoropolyether elastomer</subject><subject>Polydimethylsiloxane</subject><subject>Primary rat hepatocytes</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkEtLxDAUhYMoOI7-BCFLN615ttOVDIMvGHChrkOa3DopaVOTVph_b4e6d3W53HMO93wI3VKSU0KL-zZ37XDQscsZYSynjDHJz9CKbkqecVEW52hFeLnJJC35JbpKqSWEFIzyFXrfDoN3Ro8u9Dg0eIDY-CnEMAR_hPEAEYPXaQwdxIRdjztnYpglzjqDbZy-cAejroN3qcM6JX1M1-ii0T7Bzd9co8-nx4_dS7Z_e37dbfeZEVKOWdVowzcCjNSmFISBsdYyJvi8GS5rWWnJasNoNd80CGptI-qKaQ2FsFTzNbpbcocYvidIo-pcMuC97iFMSbGSkYoTSvkslYt0fj6lCI0aout0PCpK1AmiatUfRHWCqBaIs-9h8cHc48dBVMk46A1YF8GMygb3T8IvpmOAJw</recordid><startdate>20221105</startdate><enddate>20221105</enddate><creator>Wang, Mengyang</creator><creator>Tsuda, Masahiro</creator><creator>Deguchi, Sayaka</creator><creator>Higuchi, Yuriko</creator><creator>So, Kanako</creator><creator>Torisawa, Yu-suke</creator><creator>Takayama, Kazuo</creator><creator>Yamashita, Fumiyoshi</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20221105</creationdate><title>Application of perfluoropolyether elastomers in microfluidic drug metabolism assays</title><author>Wang, Mengyang ; Tsuda, Masahiro ; Deguchi, Sayaka ; Higuchi, Yuriko ; So, Kanako ; Torisawa, Yu-suke ; Takayama, Kazuo ; Yamashita, Fumiyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-9fac384ec5ac7402ecddd2243c74c35b59a52bc21902eae41ddf4b92aae64d1a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Chemical repellency</topic><topic>Hansen solubility parameters</topic><topic>Liver metabolism</topic><topic>Microfluidic device</topic><topic>Perfluoropolyether elastomer</topic><topic>Polydimethylsiloxane</topic><topic>Primary rat hepatocytes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Mengyang</creatorcontrib><creatorcontrib>Tsuda, Masahiro</creatorcontrib><creatorcontrib>Deguchi, Sayaka</creatorcontrib><creatorcontrib>Higuchi, Yuriko</creatorcontrib><creatorcontrib>So, Kanako</creatorcontrib><creatorcontrib>Torisawa, Yu-suke</creatorcontrib><creatorcontrib>Takayama, Kazuo</creatorcontrib><creatorcontrib>Yamashita, Fumiyoshi</creatorcontrib><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>Wang, Mengyang</au><au>Tsuda, Masahiro</au><au>Deguchi, Sayaka</au><au>Higuchi, Yuriko</au><au>So, Kanako</au><au>Torisawa, Yu-suke</au><au>Takayama, Kazuo</au><au>Yamashita, Fumiyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Application of perfluoropolyether elastomers in microfluidic drug metabolism assays</atitle><jtitle>International journal of pharmaceutics</jtitle><date>2022-11-05</date><risdate>2022</risdate><volume>627</volume><spage>122253</spage><epage>122253</epage><pages>122253-122253</pages><artnum>122253</artnum><issn>0378-5173</issn><eissn>1873-3476</eissn><abstract>[Display omitted] •Perfluoropolyether elastomers are useful in the fabrication of microfluidic devices.•Perfluoropolyether elastomers exhibit high biocompatibility and chemical repellency.•Hansen solubility parameters predict drug sorption into device materials.•Microfluidic flow improves cellular function and metabolic activity of cultured hepatocytes. Recently, increasing attention has been paid to liver-on-a-chip models for both pharmacokinetics and toxicity (ADMET) screenings. Although polydimethylsiloxane (PDMS) is the most popular material for the fabrication of microfluidic devices, its extensive sorption of hydrophobic drugs limits its applications. Therefore, we investigated a chemically repellent material, perfluoropolyether (PFPE) elastomer, as an alternative to PDMS. Primary rat hepatocytes cultured in the PFPE microfluidic device were polygonal or cuboidal in shape and had one or two prominent nuclei, as when cultured in 96-well plates. When hepatocytes were cultured in the PFPE microfluidic device and exposed to dynamic flow, the production of albumin and urea increased 3.94- and 1.72-fold, respectively, compared with no dynamic flow. Exposure to dynamic flow did not result in obvious changes in the expression of cytochrome P450, but increased the metabolic activity of hepatocytes compared to under static conditions. 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subjects Chemical repellency
Hansen solubility parameters
Liver metabolism
Microfluidic device
Perfluoropolyether elastomer
Polydimethylsiloxane
Primary rat hepatocytes
title Application of perfluoropolyether elastomers in microfluidic drug metabolism assays
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