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| Content Provider | Royal Society of Chemistry (RSC) |
|---|---|
| Author | Rillahan, Cory D. Rangarajan, Janani Fokin, Valery V. Arlian, Britni M. He, Yuan Paulson, James C. Macauley, Matthew S. Schwartz, Erik McBride, Ryan |
| Copyright Year | 2014 |
| Abstract | The siglec family of sialic acid-binding proteins are endocytic immune cell receptors that are recognized as potential targets for cell directed therapies. CD33 and CD22 are prototypical members and are validated candidates for targeting acute myeloid leukaemia and non-Hodgkin's lymphomas due to their restricted expression on myeloid cells and B-cells, respectively. While nanoparticles decorated with high affinity siglec ligands represent an attractive platform for delivery of therapeutic agents to these cells, a lack of ligands with suitable affinity and/or selectivity has hampered progress. Herein we describe selective ligands for both of these siglecs, which when displayed on liposomal nanoparticles, can efficiently target the cells expressing them in peripheral human blood. Key to their identification was the development of a facile method for chemo-enzymatic synthesis of disubstituted sialic acid analogues, combined with iterative rounds of synthesis and rapid functional analysis using glycan microarrays. |
| Starting Page | 2398 |
| Ending Page | 2406 |
| Page Count | 9 |
| File Format | HTM / HTML PDF |
| ISSN | 20416520 |
| Volume Number | 5 |
| Issue Number | 6 |
| Journal | Chemical Science |
| DOI | 10.1039/c4sc00451e |
| Language | English |
| Publisher | Royal Society of Chemistry |
| Access Restriction | Open |
| Subject Keyword | SIGLEC Myeloid tissue Carboxylic acid Functional analysis Acute myeloid leukemia CD33 CD22 Glycan |
| Content Type | Text |
| Resource Type | Article |
| Subject | Chemistry |
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