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Polyethylene Glycol Cross-Linked Hydrogel for Drug Absorption Properties
Three-dimensional polymeric networks called hydrogels have drawn a lot of interest in a variety of biomedical applications because of their distinctive qualities, like high water content and biocompatibility. Hydrogels can be strengthened mechanically and become more stable via cross-linking. In thi...
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Published in: | Journal of pharmacy & bioallied science 2024-04, Vol.16 (Suppl 2), p.S1201-S1203 |
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creator | Durairaj, Vta Kalpana, R Kumar, Vinay |
description | Three-dimensional polymeric networks called hydrogels have drawn a lot of interest in a variety of biomedical applications because of their distinctive qualities, like high water content and biocompatibility. Hydrogels can be strengthened mechanically and become more stable via cross-linking. In this study, we described the synthesis and characterization of a cross-linked hydrogel made of polyethylene glycol (PEG) capable of absorbing drug. The hydrogel was created by using a polymerization procedure to cross-link PEG chains. In order to allay this worry, we added particular functional groups to the hydrogel matrix that had a strong affinity for glutaraldehyde. These functional groups made it easier for excess glutaraldehyde to be absorbed and sequestered inside the hydrogel, lowering its cytotoxic potential. After incubation with the hydrogel, the residual glutaraldehyde concentration in solution was measured in order to assess the glutaraldehyde absorption potential. |
doi_str_mv | 10.4103/jpbs.jpbs_540_23 |
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This article is published under (http://creativecommons.org/licenses/by-nc-sa/3.0/) (the “License”). 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Hydrogels can be strengthened mechanically and become more stable via cross-linking. In this study, we described the synthesis and characterization of a cross-linked hydrogel made of polyethylene glycol (PEG) capable of absorbing drug. The hydrogel was created by using a polymerization procedure to cross-link PEG chains. In order to allay this worry, we added particular functional groups to the hydrogel matrix that had a strong affinity for glutaraldehyde. These functional groups made it easier for excess glutaraldehyde to be absorbed and sequestered inside the hydrogel, lowering its cytotoxic potential. After incubation with the hydrogel, the residual glutaraldehyde concentration in solution was measured in order to assess the glutaraldehyde absorption potential.</description><subject>Biocompatibility</subject><subject>characterization</subject><subject>Chemical properties</subject><subject>Crosslinked polymers</subject><subject>Cytotoxicity</subject><subject>Glutaraldehyde</subject><subject>human and well being</subject><subject>hydrogel</subject><subject>Hydrogels</subject><subject>life on land</subject><subject>Original</subject><subject>pegda</subject><subject>Polyethylene glycol</subject><subject>Water content</subject><issn>0976-4879</issn><issn>0975-7406</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNptUkFv0zAUjhCITWN3TigSFy4pdmzHzydUFVgnVWIHOFuO_ZKlpHGxk0n99zjtGCvClmzr-fu-5_f8ZdlbShacEvZxu6_jYl604ESX7EV2SZQUheSkenk8VwUHqS6y6xi3JA2mSkXZ6-yCAUAJAi6z9Z3vDzjeH3ocML_pD9b3-Sr4GItNN_xEl68PLvgW-7zxIf8cpjZf1tGH_dj5Ib8Lfo9h7DC-yV41po94_bhfZT--fvm-Whebbze3q-WmsILSsTBMEFILJQQ4oYA2vHIVQkUtM2BrxJJVTglpiEJwUNVosLG8BIoSa96wq-z2pOu82ep96HYmHLQ3nT4GfGi1SQ-yPWoCZSlrKi1I5EoCyNIx2jCkteMNYNL6dNLaT_UOncVhDKY_Ez2_Gbp73foHTSmVvFSQFD48KgT_a8I46l0XLfa9GdBPUTNSqQRlhCXo-3-gWz-FIfVKs6THBUiq_qJakyrohsanxHYW1UugqWtUlHPaxX9QaTrcddYP2HQpfkYgJ4KdvzZg81QkJXp2kz4a6ZmbEuXd8-Y8Ef54h_0G9M3Glw</recordid><startdate>202404</startdate><enddate>202404</enddate><creator>Durairaj, Vta</creator><creator>Kalpana, R</creator><creator>Kumar, Vinay</creator><general>Medknow Publications and Media Pvt. 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Hydrogels can be strengthened mechanically and become more stable via cross-linking. In this study, we described the synthesis and characterization of a cross-linked hydrogel made of polyethylene glycol (PEG) capable of absorbing drug. The hydrogel was created by using a polymerization procedure to cross-link PEG chains. In order to allay this worry, we added particular functional groups to the hydrogel matrix that had a strong affinity for glutaraldehyde. These functional groups made it easier for excess glutaraldehyde to be absorbed and sequestered inside the hydrogel, lowering its cytotoxic potential. After incubation with the hydrogel, the residual glutaraldehyde concentration in solution was measured in order to assess the glutaraldehyde absorption potential.</abstract><cop>India</cop><pub>Medknow Publications and Media Pvt. Ltd</pub><pmid>38882858</pmid><doi>10.4103/jpbs.jpbs_540_23</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biocompatibility characterization Chemical properties Crosslinked polymers Cytotoxicity Glutaraldehyde human and well being hydrogel Hydrogels life on land Original pegda Polyethylene glycol Water content |
title | Polyethylene Glycol Cross-Linked Hydrogel for Drug Absorption Properties |
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