<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(20)</volume><submitter>Liu N</submitter><pubmed_abstract>The origin of complex hierarchical superstructures of biomaterials and their unique self-assembly mechanisms of formation are important in biological systems and have attracted considerable attention. In the present study, we investigated the morphological changes of calcium oxalate (CaO &lt;sub>&lt;i>x&lt;/i>&lt;/sub> ) crystals induced by additives including chiral aspartic acid, sodium citrate, Mg&lt;sup>2+&lt;/sup>, casein and combinations of these molecules. The morphology and structure of CaO &lt;sub>&lt;i>x&lt;/i>&lt;/sub> were identified with the use of various techniques. The morphogenesis of CaO &lt;sub>&lt;i>x&lt;/i>&lt;/sub> crystals were significantly affected by chiral aspartic acid, sodium citrate or Mg&lt;sup>2+&lt;/sup>. However, they only formed calcium oxalate monohydrate (COM). It was observed that the chiral aspartic acid, sodium citrate and casein adhered to the surface of the crystals. The adherence of Mg&lt;sup>2+&lt;/sup> to crystals was not evident. Casein significantly affected the formation of COM and calcium oxalate dihydrate (COD). The ratio of different CaO &lt;sub>&lt;i>x&lt;/i>&lt;/sub> crystal forms is associated with the casein concentration. In combination with Mg&lt;sup>2+&lt;/sup> or citrate ions, casein showed improved formation of COD. The present study mimics biomineralization with a simple chemical approach and provides insight into the complicated system of CaO &lt;sub>&lt;i>x&lt;/i>&lt;/sub> biomineralization as well as facilitates the understanding of urinary stone treatment.</pubmed_abstract><journal>RSC advances</journal><pagination>11014-11020</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9078945</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Shape and structure controlling of calcium oxalate crystals by a combination of additives in the process of biomineralization.</pubmed_title><pmcid>PMC9078945</pmcid><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Ping H</pubmed_authors><pubmed_authors>Guo J</pubmed_authors><pubmed_authors>Xie H</pubmed_authors><pubmed_authors>Tao F</pubmed_authors><pubmed_authors>Liu N</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>Su BL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Shape and structure controlling of calcium oxalate crystals by a combination of additives in the process of biomineralization.</name><description>The origin of complex hierarchical superstructures of biomaterials and their unique self-assembly mechanisms of formation are important in biological systems and have attracted considerable attention. In the present study, we investigated the morphological changes of calcium oxalate (CaO &lt;sub>&lt;i>x&lt;/i>&lt;/sub> ) crystals induced by additives including chiral aspartic acid, sodium citrate, Mg&lt;sup>2+&lt;/sup>, casein and combinations of these molecules. The morphology and structure of CaO &lt;sub>&lt;i>x&lt;/i>&lt;/sub> were identified with the use of various techniques. The morphogenesis of CaO &lt;sub>&lt;i>x&lt;/i>&lt;/sub> crystals were significantly affected by chiral aspartic acid, sodium citrate or Mg&lt;sup>2+&lt;/sup>. However, they only formed calcium oxalate monohydrate (COM). It was observed that the chiral aspartic acid, sodium citrate and casein adhered to the surface of the crystals. The adherence of Mg&lt;sup>2+&lt;/sup> to crystals was not evident. Casein significantly affected the formation of COM and calcium oxalate dihydrate (COD). The ratio of different CaO &lt;sub>&lt;i>x&lt;/i>&lt;/sub> crystal forms is associated with the casein concentration. In combination with Mg&lt;sup>2+&lt;/sup> or citrate ions, casein showed improved formation of COD. The present study mimics biomineralization with a simple chemical approach and provides insight into the complicated system of CaO &lt;sub>&lt;i>x&lt;/i>&lt;/sub> biomineralization as well as facilitates the understanding of urinary stone treatment.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Mar</publication><modification>2025-04-29T10:58:59.1Z</modification><creation>2024-10-15T07:28:38.161Z</creation></dates><accession>S-EPMC9078945</accession><cross_references><pubmed>35541543</pubmed><doi>10.1039/c8ra00661j</doi></cross_references></HashMap>