<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Avicenna Journal of Pharmaceutical Research</title>
<title_fa>Avicenna Journal of Pharmaceutical Research</title_fa>
<short_title>Avicenna J Pharma Res</short_title>
<subject>Medical Sciences</subject>
<web_url>http://ajpr1.umsha.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></journal_id_issn>
<journal_id_issn_online>2717-1884</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.53208</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1399</year>
	<month>5</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2020</year>
	<month>8</month>
	<day>1</day>
</pubdate>
<volume>1</volume>
<number>1</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>Preparation, Box-Behnken Statistical Optimization, and In Vitro Characterization of a Self-nanoemulsifying Drug Delivery System for the Oral Delivery of Budesonide as a Poorly Soluble Drug</title>
	<subject_fa>عمومى</subject_fa>
	<subject>General</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Research</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p&gt;&lt;strong&gt;Background&lt;/strong&gt;: Self-nanoemulsifying drug delivery systems (SNEDDS) can be used to improve the oral bioavailability of lipophilic drugs. The aim of this study was the preparation and characterization of a SNEDDS for the oral delivery of budesonide as a poorly soluble drug.&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;Methods&lt;/strong&gt;: To prepare SNEDDS, budesonide (20 mg) was dissolved in the mixture of liquid paraffin, Tween 80, and propylene glycol, followed by using the Box-Behnken response surface methodology for statistical optimization. The prepared mixtures were then diluted in the simulated intestinal fluid (SIF) and their physico-chemical characteristics were studied as well. Then, SNEDDS were morphologically evaluated using transmission electron microscopy (TEM). Finally, the &lt;em&gt;in vitro&lt;/em&gt; release profile of budesonide from nano-droplets was determined in the SIF.&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;Results&lt;/strong&gt;: Based on the results, the size, polydispersity index, zeta potential, and entrapment efficiency of statistically optimized SNEEDS were reported as 146&amp;plusmn;37 nm, 0.211&amp;plusmn;0.06, +3.6&amp;plusmn;0.84 mV, and 94.3&amp;plusmn;6.58%, respectively. In addition, TEM images revealed spherical nano-droplets. Further, the release profile of budesonide from nano-droplets exhibited 33.81&amp;plusmn;1.67% of drug release in SIF during 360 minutes of incubation at 37&amp;deg; C, indicating sustained drug release.&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;Conclusion&lt;/strong&gt;: The obtained data demonstrated that SNEDDS could be regarded as a good candidate for oral delivery of budesonide as a poorly water-soluble drug representing a high first-pass metabolism.&lt;/p&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Budesonide, Poorly water-soluble drugs, Self-nanoemulsifying drug delivery system, Oral delivery, Lymphatic absorption, Statistical optimization</keyword>
	<start_page>24</start_page>
	<end_page>32</end_page>
	<web_url>http://ajpr1.umsha.ac.ir/browse.php?a_code=A-10-2-27&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Sahar </first_name>
	<middle_name></middle_name>
	<last_name>Khoshyari </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>1003194753284600165</code>
	<orcid>1003194753284600165</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Pharmaceutics, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Reza </first_name>
	<middle_name></middle_name>
	<last_name>Mahjub</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> r.mahjoub@umsha.ac.ir</email>
	<code>1003194753284600166</code>
	<orcid>1003194753284600166</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Pharmaceutics, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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