<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE Articles SYSTEM "HBI_DTD">
<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>1</Volume><Issue>3</Issue></Journal><ArticleTitle>DISSOLUTION CHARACTERISTIC OF CHLORAMPHENICOL PALMITATE-LIPOSOMAL PREPARATION</ArticleTitle><FirstPage>1</FirstPage><LastPage>8</LastPage><AuthorList><Author><FirstName></FirstName><LastName>Morteza Rafiee-Tehrani</LastName></Author><Author><FirstName></FirstName><LastName>Zahra Tolouii-Barazandeh</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2015</Year><Month>10</Month><Day>06</Day></PubDate></History><Abstract>Solid dispersions of chloramphenicol palmitate and dipalmitoyl-phosphatidylcholine (lecithin) have been produced both as copreci-pitate and physical mixtures. The dissolution behavior of both forms were compared with pure chloramphenicol palrnitate st different weight ratios of chloramphenicol palrnitate-lecithin (liposomal system); as well as various pH. The dissolution characteristic of physical mixtures for different weight ratios of chloramphenicol palmitate-lecithin was similar to the pure drug. Whereas, the coprecipitates produced a 2.8 fold greater initial dissolution rate (1DR) and a 2.4 fold greater drug release concentration after 60 min at a chloramphenicol palmitatc-lecithin weight ratio of 19:1. However, lecithin content enhancement to 9:1, 4:1 and 1.5:1 compositions, resulted in a further increase of 6%, 21%. and 24%. respectively in the initial dissolution rate. In&amp;not;creasing the lecithin content shows only a slight increase (8.5&amp;deg;c) on drug release after 60 min when, the chloramphenicol palrnitate lecithin weight ratio was 1.5:1. However, other weight ratios did not show any effect on the improvement of drug release after 60 min. I he effect of pH of the medium on dissolution was slight, but varied with composition of the system.In conclusion, liposome encapsulation of chloramphenicol palmitale has a significant effect on dissolution improvement of this drug.</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/22</web_url><pdf_url>https://daru.tums.ac.ir/index.php/daru/article/download/22/22</pdf_url></Article></Articles>
