<?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>Assessing the bioadhesivity of Acconon MC 8-2 EP/NF for gastroretention of floating microsponges of loratadine and achieving controlled drug delivery </title>
	<subject_fa>فارماسیوتیکس</subject_fa>
	<subject>Pharmaceutics</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Original Research</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p&gt;The aim of the present work was to assess the feasibility of Acconon MC8-2 EP/NF as a bioadhesive material for developing controlled release gastroretentive microsponges of loratadine. Modified emulsion-solvent diffusion method was employed for the preparation of microsponges (F1-F9) based on &amp;nbsp;3&lt;sup&gt;2&lt;/sup&gt; factorial design. The amount of ethyl cellulose (EC) and polyvinyl alcohol (PVA) were selected as independent variables while particle size, entrapment efficiency and %CDR were designated as dependent variables. The formulation (F1) with least particle size of 54 &amp;plusmn; 2.37&amp;micro;m, entrapment efficiency of 65.98 &amp;plusmn; 2.21 % and CDR of 88.15 &amp;plusmn; 1.59% at 8 h that followed zero order release kinetics was selected as optimized formulation. F1 was re-fabricated as bioadhesive microsponges (BF1) using Acconon MC 8-2 and assessed.&amp;nbsp; The particle size of BF1increased to 84 &amp;plusmn; 2.29 &amp;micro;m whereas the entrapment efficiency lowered to 55.19 &amp;plusmn; 1.36% in comparison to F1. However, the CDR&lt;sub&gt;8h&lt;/sub&gt; from BF1 (81.65 &amp;plusmn; 3.37%) was comparable to F1. Dynamic &lt;em&gt;in vitro&lt;/em&gt; bioadhesion test confirmed the bioadhesive property of BF1. &lt;em&gt;Ex vivo&lt;/em&gt; permeation across gastric mucin depicted 52.87% CDP&lt;sub&gt;8h&lt;/sub&gt; that followed zero order kinetics (r&lt;sup&gt;2&lt;/sup&gt; = 0.9885). Scanning electron microscopy revealed spherical and highly porous surface. The FTIR studies revealed no chemical interaction between drug and excipients. Hence, the study affirmed the bioadhesive characteristics of Acconon MC 8-2 EP/NF for development of controlled release biaodhesive floating microsponges of loratadine.&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Acconon MC 8-2 EP/NF, bioadhesivity, loratadine, gastroretentive microsponges</keyword>
	<start_page>58</start_page>
	<end_page>74</end_page>
	<web_url>http://pbr.mazums.ac.ir/browse.php?a_code=A-10-53-4&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Sonam</first_name>
	<middle_name></middle_name>
	<last_name>Singh</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>1003194753284600975</code>
	<orcid>1003194753284600975</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Pharmaceutics, Rajiv Academy for Pharmacy, Mathura, 281001, India</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Kamla</first_name>
	<middle_name></middle_name>
	<last_name>Pathak</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>1003194753284600976</code>
	<orcid>1003194753284600976</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Pharmaceutics, Pharmacy College Saifai, Uttar Pradesh University of Medical Sciences, Saifai, Etawah, 206130, India</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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