<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Master A</submitter><funding>Stony Brook University</funding><funding>NEI NIH HHS</funding><funding>National Institutes of Health</funding><pagination>41-50</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8792174</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>47(1)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>To develop a more efficient impression cytology (IC) method for the transfer of ocular surface cells onto glass microscope slides for cytochemical, immunocytochemical, and immunofluorescence studies.&lt;h4>Methods&lt;/h4>Cells are lifted off the ocular surface with a mixed cellulose ester membrane and then firmly attached to a glass slide using a novel triblock copolymer comprised of collagen type I, polyethylenimine and poly-L-lysine (CPP), and crosslinking cells and glass slide by heating and cooling. The membrane is removed intact after softening it with a butanol/ethanol solution. Transfer of cells is complete in about 10-15 minutes and is ready for staining. The efficiency of our cell transfer method was compared to current methods based on poly-L-lysine and albumin paste.&lt;h</pubmed_abstract><journal>Current eye research</journal><pubmed_title>An Improved Ocular Impression Cytology Method: Quantitative Cell Transfer to Microscope Slides Using a Novel Polymer.</pubmed_title><pmcid>PMC8792174</pmcid><funding_grant_id>R44 EY031193</funding_grant_id><funding_grant_id>R44EY031193</funding_grant_id><pubmed_authors>Rigas B</pubmed_authors><pubmed_authors>Master A</pubmed_authors><pubmed_authors>Huang W</pubmed_authors><pubmed_authors>Huang L</pubmed_authors><pubmed_authors>Honkanen R</pubmed_authors></additional><is_claimable>false</is_claimable><name>An Improved Ocular Impression Cytology Method: Quantitative Cell Transfer to Microscope Slides Using a Novel Polymer.</name><description>&lt;h4>Purpose&lt;/h4>To develop a more efficient impression cytology (IC) method for the transfer of ocular surface cells onto glass microscope slides for cytochemical, immunocytochemical, and immunofluorescence studies.&lt;h4>Methods&lt;/h4>Cells are lifted off the ocular surface with a mixed cellulose ester membrane and then firmly attached to a glass slide using a novel triblock copolymer comprised of collagen type I, polyethylenimine and poly-L-lysine (CPP), and crosslinking cells and glass slide by heating and cooling. The membrane is removed intact after softening it with a butanol/ethanol solution. Transfer of cells is complete in about 10-15 minutes and is ready for staining. The efficiency of our cell transfer method was compared to current methods based on poly-L-lysine and albumin paste.&lt;h</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2025-08-30T03:08:16.867Z</modification><creation>2025-04-06T09:40:55.602Z</creation></dates><accession>S-EPMC8792174</accession><cross_references><pubmed>34841993</pubmed><doi>10.1080/02713683.2021.1951300</doi></cross_references></HashMap>