Nanocrystal-based gel of apremilast ameliorates imiquimod-induced psoriasis by suppressing inflammatory responses
[Display omitted] •Nanocrystal is a promising approach for ‘difficult-to-deliver’ drugs such as apremilast.•Nanocrystal-based gel enhanced the therapeutic efficacy of apremilast in the management of psoriasis.•Skin irritation study showed significantly less irritation potential of a nanocrystal-base...
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Veröffentlicht in: | International journal of pharmaceutics 2022-06, Vol.622, p.121873-121873, Article 121873 |
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creator | Parmar, Prashantkumar K. Sharma, Nisha Wasil Kabeer, Shaheen Rohit, Aastha Bansal, Arvind K. |
description | [Display omitted]
•Nanocrystal is a promising approach for ‘difficult-to-deliver’ drugs such as apremilast.•Nanocrystal-based gel enhanced the therapeutic efficacy of apremilast in the management of psoriasis.•Skin irritation study showed significantly less irritation potential of a nanocrystal-based gel than the positive control.
Apremilast is ‘difficult-to-deliver’ in stratum corneum and viable layers (viable epidermis, dermis) owing to its modest lipophilicity and poor aqueous solubility, respectively. The objective of the present research was to develop apremilast nanocrystal-based gel for enhanced anti-psoriatic efficacy for the treatment of psoriasis. Nanosuspension was generated by wet media milling with a mean particle size of 200 nm. In-vivoefficacy of nanocrystal-based gels was evaluated in the imiquimod-induced psoriatic plaque model. Nanocrystal-based gel (1% and 3% w/w) improved phenotypic, histopathological features of psoriatic skin and attenuated splenic hypertrophy, psoriasis area severity scoring. Enzyme-linked immunosorbent assay was performed to evaluate levels of psoriatic biochemical markers indicating a significant decrease in the concentration of cytokines such as IL-23, IL-17A, IL-6 and TNF-α by nanocrystal-based gels (1% and 3% w/w) over disease induced group. Skin irritation study revealed that nanocrystal-based gel was significantly less irritating than the positive control. These results suggest that nanocrystal-based gel of apremilast can be an effective strategy for the management of psoriasis. |
doi_str_mv | 10.1016/j.ijpharm.2022.121873 |
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•Nanocrystal is a promising approach for ‘difficult-to-deliver’ drugs such as apremilast.•Nanocrystal-based gel enhanced the therapeutic efficacy of apremilast in the management of psoriasis.•Skin irritation study showed significantly less irritation potential of a nanocrystal-based gel than the positive control.
Apremilast is ‘difficult-to-deliver’ in stratum corneum and viable layers (viable epidermis, dermis) owing to its modest lipophilicity and poor aqueous solubility, respectively. The objective of the present research was to develop apremilast nanocrystal-based gel for enhanced anti-psoriatic efficacy for the treatment of psoriasis. Nanosuspension was generated by wet media milling with a mean particle size of 200 nm. In-vivoefficacy of nanocrystal-based gels was evaluated in the imiquimod-induced psoriatic plaque model. Nanocrystal-based gel (1% and 3% w/w) improved phenotypic, histopathological features of psoriatic skin and attenuated splenic hypertrophy, psoriasis area severity scoring. Enzyme-linked immunosorbent assay was performed to evaluate levels of psoriatic biochemical markers indicating a significant decrease in the concentration of cytokines such as IL-23, IL-17A, IL-6 and TNF-α by nanocrystal-based gels (1% and 3% w/w) over disease induced group. Skin irritation study revealed that nanocrystal-based gel was significantly less irritating than the positive control. These results suggest that nanocrystal-based gel of apremilast can be an effective strategy for the management of psoriasis.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2022.121873</identifier><identifier>PMID: 35640806</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Apremilast ; Imiquimod-induced psoriatic plaque model ; Nanocrystal-based gel ; Psoriasis ; Topical delivery</subject><ispartof>International journal of pharmaceutics, 2022-06, Vol.622, p.121873-121873, Article 121873</ispartof><rights>2022 Elsevier B.V.</rights><rights>Copyright © 2022 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-5d60dd72aa0a22a9b8916bcca3ebe1a3cbfd233807b49d3985500155f0699f633</citedby><cites>FETCH-LOGICAL-c365t-5d60dd72aa0a22a9b8916bcca3ebe1a3cbfd233807b49d3985500155f0699f633</cites><orcidid>0000-0002-7593-2676 ; 0000-0002-3182-7559 ; 0000-0001-6051-6680</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0378517322004288$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35640806$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Parmar, Prashantkumar K.</creatorcontrib><creatorcontrib>Sharma, Nisha</creatorcontrib><creatorcontrib>Wasil Kabeer, Shaheen</creatorcontrib><creatorcontrib>Rohit, Aastha</creatorcontrib><creatorcontrib>Bansal, Arvind K.</creatorcontrib><title>Nanocrystal-based gel of apremilast ameliorates imiquimod-induced psoriasis by suppressing inflammatory responses</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><description>[Display omitted]
•Nanocrystal is a promising approach for ‘difficult-to-deliver’ drugs such as apremilast.•Nanocrystal-based gel enhanced the therapeutic efficacy of apremilast in the management of psoriasis.•Skin irritation study showed significantly less irritation potential of a nanocrystal-based gel than the positive control.
Apremilast is ‘difficult-to-deliver’ in stratum corneum and viable layers (viable epidermis, dermis) owing to its modest lipophilicity and poor aqueous solubility, respectively. The objective of the present research was to develop apremilast nanocrystal-based gel for enhanced anti-psoriatic efficacy for the treatment of psoriasis. Nanosuspension was generated by wet media milling with a mean particle size of 200 nm. In-vivoefficacy of nanocrystal-based gels was evaluated in the imiquimod-induced psoriatic plaque model. Nanocrystal-based gel (1% and 3% w/w) improved phenotypic, histopathological features of psoriatic skin and attenuated splenic hypertrophy, psoriasis area severity scoring. Enzyme-linked immunosorbent assay was performed to evaluate levels of psoriatic biochemical markers indicating a significant decrease in the concentration of cytokines such as IL-23, IL-17A, IL-6 and TNF-α by nanocrystal-based gels (1% and 3% w/w) over disease induced group. Skin irritation study revealed that nanocrystal-based gel was significantly less irritating than the positive control. These results suggest that nanocrystal-based gel of apremilast can be an effective strategy for the management of psoriasis.</description><subject>Apremilast</subject><subject>Imiquimod-induced psoriatic plaque model</subject><subject>Nanocrystal-based gel</subject><subject>Psoriasis</subject><subject>Topical delivery</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkE1v1DAQhi1ERbeFnwDykUsWf6yd5IRQBS1SBZdytib2pHgVx1lPgrT_nqx26ZXTSKPnnVfzMPZeiq0U0n7ab-N--g0lbZVQaiuVbGr9im1Oo9K72r5mG6HrpjKy1tfshmgvhLBK6jfsWhu7E42wG3b4AWP25UgzDFUHhIE_48Bzz2EqmOIANHNIOMRcYEbiMcXDElMOVRzD4ld-olwiUCTeHTkt05ojiuMzj2M_QEow53Lk63LKIyG9ZVc9DITvLvOW_fr29enuoXr8ef_97stj5bU1c2WCFSHUCkCAUtB2TStt5z1o7FCC9l0flNaNqLtdG3TbGCOENKYXtm17q_Ut-3i-O5V8WJBmlyJ5HAYYMS_klK2VVqpRzYqaM-pLJirYu6nEBOXopHAn227vLrbdybY7215zHy4VS5cwvKT-6V2Bz2cA10f_RCyOfMRxtRYL-tmFHP9T8RcK4ZZn</recordid><startdate>20220625</startdate><enddate>20220625</enddate><creator>Parmar, Prashantkumar K.</creator><creator>Sharma, Nisha</creator><creator>Wasil Kabeer, Shaheen</creator><creator>Rohit, Aastha</creator><creator>Bansal, Arvind K.</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7593-2676</orcidid><orcidid>https://orcid.org/0000-0002-3182-7559</orcidid><orcidid>https://orcid.org/0000-0001-6051-6680</orcidid></search><sort><creationdate>20220625</creationdate><title>Nanocrystal-based gel of apremilast ameliorates imiquimod-induced psoriasis by suppressing inflammatory responses</title><author>Parmar, Prashantkumar K. ; Sharma, Nisha ; Wasil Kabeer, Shaheen ; Rohit, Aastha ; Bansal, Arvind K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-5d60dd72aa0a22a9b8916bcca3ebe1a3cbfd233807b49d3985500155f0699f633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Apremilast</topic><topic>Imiquimod-induced psoriatic plaque model</topic><topic>Nanocrystal-based gel</topic><topic>Psoriasis</topic><topic>Topical delivery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Parmar, Prashantkumar K.</creatorcontrib><creatorcontrib>Sharma, Nisha</creatorcontrib><creatorcontrib>Wasil Kabeer, Shaheen</creatorcontrib><creatorcontrib>Rohit, Aastha</creatorcontrib><creatorcontrib>Bansal, Arvind K.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Parmar, Prashantkumar K.</au><au>Sharma, Nisha</au><au>Wasil Kabeer, Shaheen</au><au>Rohit, Aastha</au><au>Bansal, Arvind K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nanocrystal-based gel of apremilast ameliorates imiquimod-induced psoriasis by suppressing inflammatory responses</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2022-06-25</date><risdate>2022</risdate><volume>622</volume><spage>121873</spage><epage>121873</epage><pages>121873-121873</pages><artnum>121873</artnum><issn>0378-5173</issn><eissn>1873-3476</eissn><abstract>[Display omitted]
•Nanocrystal is a promising approach for ‘difficult-to-deliver’ drugs such as apremilast.•Nanocrystal-based gel enhanced the therapeutic efficacy of apremilast in the management of psoriasis.•Skin irritation study showed significantly less irritation potential of a nanocrystal-based gel than the positive control.
Apremilast is ‘difficult-to-deliver’ in stratum corneum and viable layers (viable epidermis, dermis) owing to its modest lipophilicity and poor aqueous solubility, respectively. The objective of the present research was to develop apremilast nanocrystal-based gel for enhanced anti-psoriatic efficacy for the treatment of psoriasis. Nanosuspension was generated by wet media milling with a mean particle size of 200 nm. In-vivoefficacy of nanocrystal-based gels was evaluated in the imiquimod-induced psoriatic plaque model. Nanocrystal-based gel (1% and 3% w/w) improved phenotypic, histopathological features of psoriatic skin and attenuated splenic hypertrophy, psoriasis area severity scoring. Enzyme-linked immunosorbent assay was performed to evaluate levels of psoriatic biochemical markers indicating a significant decrease in the concentration of cytokines such as IL-23, IL-17A, IL-6 and TNF-α by nanocrystal-based gels (1% and 3% w/w) over disease induced group. Skin irritation study revealed that nanocrystal-based gel was significantly less irritating than the positive control. These results suggest that nanocrystal-based gel of apremilast can be an effective strategy for the management of psoriasis.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>35640806</pmid><doi>10.1016/j.ijpharm.2022.121873</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-7593-2676</orcidid><orcidid>https://orcid.org/0000-0002-3182-7559</orcidid><orcidid>https://orcid.org/0000-0001-6051-6680</orcidid></addata></record> |
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subjects | Apremilast Imiquimod-induced psoriatic plaque model Nanocrystal-based gel Psoriasis Topical delivery |
title | Nanocrystal-based gel of apremilast ameliorates imiquimod-induced psoriasis by suppressing inflammatory responses |
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