<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Pharmaceutical and Biomedical Research</title>
<title_fa></title_fa>
<short_title>Pharm Biomed Res</short_title>
<subject>Medical Sciences</subject>
<web_url>http://pbr.mazums.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2423-4486</journal_id_issn>
<journal_id_issn_online>2423-4494</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.29252/pbr</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1395</year>
	<month>3</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2016</year>
	<month>6</month>
	<day>1</day>
</pubdate>
<volume>2</volume>
<number>2</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Comparative in vitro assessment of tolterodine tartrate tablets by high performance liquid chromatographic (HPLC)</title>
	<subject_fa>داروسازی صنعتی</subject_fa>
	<subject>Industrial Pharmacy</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Original Research</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p&gt;Tolterodine tartrate, is a new, potent and competitive muscarinic receptor antagonist in clinical development for the treatment of urge incontinence and other symptoms of unstable bladder. The purpose of this study is to establish a reliable and quick method for the assignment of tolterodine tartrate by high performance liquid chromatography with ultraviolet detection (HPLC-UV). A rapid&amp;nbsp; and&amp;nbsp; sensitive&amp;nbsp; high&amp;nbsp; performance&amp;nbsp; liquid&amp;nbsp; chromatographic&amp;nbsp; (HPLC)&amp;nbsp; method&amp;nbsp; has&amp;nbsp; been developed&amp;nbsp; for&amp;nbsp; determination&amp;nbsp; of&amp;nbsp; tolterodine tartrate.&amp;nbsp; Mobile phase was composed of phosphate acetate 0.1 M (pH 2.5)-acetonitrile (50:50 v/v) with a flow rate of 1.2 ml/min. The eluted peaks were detected by a UV detector was set at wavelength of 285 nm. The method was validated in the range of tolterodine tartrate concentrations from 10 to 100 &amp;micro;g/ml. The limits of detection (LOD) and quantitation (LOQ) of the method were 5 and 10 &amp;micro;g/ml, respectively. The average drug recovery was 98.20 % throughout the linear concentration range. The average within-run and between-run accuracy values of 98.56 % and 99.11 % respectively. Statistical&amp;nbsp; assessment&amp;nbsp; of&amp;nbsp; various&amp;nbsp; &lt;em&gt;in&amp;nbsp; vitro&lt;/em&gt;&amp;nbsp; dissolution&amp;nbsp; parameters&amp;nbsp; and&amp;nbsp; assay&amp;nbsp; results was&amp;nbsp; also&amp;nbsp; conducted&amp;nbsp; to&amp;nbsp; establish&amp;nbsp; if&amp;nbsp; there were&amp;nbsp; any significant difference among them. The validated HPLC method has been used successfully to study tolterodine tartrate.&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Tolterodine tartrate, HPLC, assay, dissolution</keyword>
	<start_page>47</start_page>
	<end_page>57</end_page>
	<web_url>http://pbr.mazums.ac.ir/browse.php?a_code=A-10-47-9&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Hossein</first_name>
	<middle_name></middle_name>
	<last_name>Danafar</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>1003194753284600974</code>
	<orcid>1003194753284600974</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Zanjan Pharmaceutical Nanotechnology Research Center, Zanjan University of Medical Sciences, Zanjan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
