Preclinical Safety Evaluation in Rats of a Polymeric Matrix Containing an siRNA Drug Used as a Local and Prolonged Delivery System for Pancreatic Cancer Therapy
Conventional chemotherapy treatments for pancreatic cancer are mainly palliative. RNA interference (RNAi)-based drugs present the potential for a new targeted treatment. LOcal Drug EluteR (LODERTM) is a novel biodegradable polymeric matrix that shields drugs against enzymatic degradation and release...
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Veröffentlicht in: | Toxicologic pathology 2016-08, Vol.44 (6), p.856-865 |
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creator | Ramot, Yuval Rotkopf, Shay Gabai, Rachel Malka Zorde Khvalevsky, Elina Muravnik, Sofia Marzoli, Gabriela Alejandra Domb, Abraham J. Shemi, Amotz Nyska, Abraham |
description | Conventional chemotherapy treatments for pancreatic cancer are mainly palliative. RNA interference (RNAi)-based drugs present the potential for a new targeted treatment. LOcal Drug EluteR (LODERTM) is a novel biodegradable polymeric matrix that shields drugs against enzymatic degradation and releases small interfering RNA (siRNA) against G12D-mutated KRAS (siG12D). siG12D-LODER has successfully passed a phase 1/2a clinical trial. Such a formulation necessitates biocompatibility and safety studies. We describe the safety and toxicity studies with siG12D-LODER in 192 Hsd:Sprague Dawley rats, after repeated subcutaneous administrations (days 1, 14, and 28). Animals were sacrificed on days 29 and 42 (recovery phase). In all groups, no adverse effects were noted, and all animals showed favorable local and systemic tolerability. Histopathologically, LODER implantation resulted in the expected capsule formation, composed of a thin fibrotic tissue. On the interface between the cavity and the capsule, a single layer composed of macrophages and multinucleated giant cells was observed. No difference was noted between the placebo and siG12D-LODER groups. These findings provide valuable information for future preclinical studies with siRNA-bearing biodegradable polymers and for the safety aspects of RNAi-based drugs as a targeted therapy. |
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RNA interference (RNAi)-based drugs present the potential for a new targeted treatment. LOcal Drug EluteR (LODERTM) is a novel biodegradable polymeric matrix that shields drugs against enzymatic degradation and releases small interfering RNA (siRNA) against G12D-mutated KRAS (siG12D). siG12D-LODER has successfully passed a phase 1/2a clinical trial. Such a formulation necessitates biocompatibility and safety studies. We describe the safety and toxicity studies with siG12D-LODER in 192 Hsd:Sprague Dawley rats, after repeated subcutaneous administrations (days 1, 14, and 28). Animals were sacrificed on days 29 and 42 (recovery phase). In all groups, no adverse effects were noted, and all animals showed favorable local and systemic tolerability. Histopathologically, LODER implantation resulted in the expected capsule formation, composed of a thin fibrotic tissue. On the interface between the cavity and the capsule, a single layer composed of macrophages and multinucleated giant cells was observed. No difference was noted between the placebo and siG12D-LODER groups. These findings provide valuable information for future preclinical studies with siRNA-bearing biodegradable polymers and for the safety aspects of RNAi-based drugs as a targeted therapy.</description><identifier>ISSN: 0192-6233</identifier><identifier>EISSN: 1533-1601</identifier><identifier>DOI: 10.1177/0192623316645860</identifier><identifier>PMID: 27147553</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Animals ; Antineoplastic Agents - pharmacology ; Carcinoma, Pancreatic Ductal - drug therapy ; Drug Carriers - pharmacology ; Lactic Acid - pharmacology ; Pancreatic Neoplasms - drug therapy ; Polyglycolic Acid - pharmacology ; Proto-Oncogene Proteins p21(ras) - antagonists & inhibitors ; Proto-Oncogene Proteins p21(ras) - genetics ; Rats ; Rats, Sprague-Dawley ; RNA, Small Interfering - pharmacology</subject><ispartof>Toxicologic pathology, 2016-08, Vol.44 (6), p.856-865</ispartof><rights>2016 by The Author(s) 2016</rights><rights>2016 by The Author(s) 2016.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-faeb7d108d235869fb2992b7ed1c97aaf21e22fae4b2adb48e15b7215fc3b0c23</citedby><cites>FETCH-LOGICAL-c478t-faeb7d108d235869fb2992b7ed1c97aaf21e22fae4b2adb48e15b7215fc3b0c23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0192623316645860$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0192623316645860$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21799,27903,27904,43600,43601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27147553$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ramot, Yuval</creatorcontrib><creatorcontrib>Rotkopf, Shay</creatorcontrib><creatorcontrib>Gabai, Rachel Malka</creatorcontrib><creatorcontrib>Zorde Khvalevsky, Elina</creatorcontrib><creatorcontrib>Muravnik, Sofia</creatorcontrib><creatorcontrib>Marzoli, Gabriela Alejandra</creatorcontrib><creatorcontrib>Domb, Abraham J.</creatorcontrib><creatorcontrib>Shemi, Amotz</creatorcontrib><creatorcontrib>Nyska, Abraham</creatorcontrib><title>Preclinical Safety Evaluation in Rats of a Polymeric Matrix Containing an siRNA Drug Used as a Local and Prolonged Delivery System for Pancreatic Cancer Therapy</title><title>Toxicologic pathology</title><addtitle>Toxicol Pathol</addtitle><description>Conventional chemotherapy treatments for pancreatic cancer are mainly palliative. RNA interference (RNAi)-based drugs present the potential for a new targeted treatment. LOcal Drug EluteR (LODERTM) is a novel biodegradable polymeric matrix that shields drugs against enzymatic degradation and releases small interfering RNA (siRNA) against G12D-mutated KRAS (siG12D). siG12D-LODER has successfully passed a phase 1/2a clinical trial. Such a formulation necessitates biocompatibility and safety studies. We describe the safety and toxicity studies with siG12D-LODER in 192 Hsd:Sprague Dawley rats, after repeated subcutaneous administrations (days 1, 14, and 28). Animals were sacrificed on days 29 and 42 (recovery phase). In all groups, no adverse effects were noted, and all animals showed favorable local and systemic tolerability. Histopathologically, LODER implantation resulted in the expected capsule formation, composed of a thin fibrotic tissue. On the interface between the cavity and the capsule, a single layer composed of macrophages and multinucleated giant cells was observed. No difference was noted between the placebo and siG12D-LODER groups. These findings provide valuable information for future preclinical studies with siRNA-bearing biodegradable polymers and for the safety aspects of RNAi-based drugs as a targeted therapy.</description><subject>Animals</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Carcinoma, Pancreatic Ductal - drug therapy</subject><subject>Drug Carriers - pharmacology</subject><subject>Lactic Acid - pharmacology</subject><subject>Pancreatic Neoplasms - drug therapy</subject><subject>Polyglycolic Acid - pharmacology</subject><subject>Proto-Oncogene Proteins p21(ras) - antagonists & inhibitors</subject><subject>Proto-Oncogene Proteins p21(ras) - genetics</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA, Small Interfering - pharmacology</subject><issn>0192-6233</issn><issn>1533-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUtv1DAUhS0EokPbPSt0l2wCtvNeVtPykAYY9bGObpzrwZVjD3ZSkX_DT61HU1hUYmVL5zvH8jmMvRX8gxB1_ZGLVlYyz0VVFWVT8RdsJco8z0TFxUu2OsjZQT9hb2K851w0ouCv2YmsRVGXZb5if7aBlDXOKLRwg5qmBa4e0M44Ge_AOLjGKYLXgLD1dhkpGAXfcArmN6y9mzB53Q7QQTTX3y_gMsw7uIs0AMbk2fhDMLoBtsFb73ZJuCRrHigscLPEiUbQPsAWnQqUHlWwTlcKcPuTAu6XM_ZKo410_nSesrtPV7frL9nmx-ev64tNpoq6mTKN1NeD4M0g89REq3vZtrKvaRCqrRG1FCRloope4tAXDYmyr6Uotcp7rmR-yt4fc_fB_5opTt1ooiJr0ZGfY5eqE02Tmm4Tyo-oCj7GQLrbBzNiWDrBu8Mu3fNdkuXdU_rcjzT8M_wdIgHZEYi4o-7ez8Gl3_4_8BHMnpbD</recordid><startdate>20160801</startdate><enddate>20160801</enddate><creator>Ramot, Yuval</creator><creator>Rotkopf, Shay</creator><creator>Gabai, Rachel Malka</creator><creator>Zorde Khvalevsky, Elina</creator><creator>Muravnik, Sofia</creator><creator>Marzoli, Gabriela Alejandra</creator><creator>Domb, Abraham J.</creator><creator>Shemi, Amotz</creator><creator>Nyska, Abraham</creator><general>SAGE Publications</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20160801</creationdate><title>Preclinical Safety Evaluation in Rats of a Polymeric Matrix Containing an siRNA Drug Used as a Local and Prolonged Delivery System for Pancreatic Cancer Therapy</title><author>Ramot, Yuval ; Rotkopf, Shay ; Gabai, Rachel Malka ; Zorde Khvalevsky, Elina ; Muravnik, Sofia ; Marzoli, Gabriela Alejandra ; Domb, Abraham J. ; Shemi, Amotz ; Nyska, Abraham</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-faeb7d108d235869fb2992b7ed1c97aaf21e22fae4b2adb48e15b7215fc3b0c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Carcinoma, Pancreatic Ductal - drug therapy</topic><topic>Drug Carriers - pharmacology</topic><topic>Lactic Acid - pharmacology</topic><topic>Pancreatic Neoplasms - drug therapy</topic><topic>Polyglycolic Acid - pharmacology</topic><topic>Proto-Oncogene Proteins p21(ras) - antagonists & inhibitors</topic><topic>Proto-Oncogene Proteins p21(ras) - genetics</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA, Small Interfering - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ramot, Yuval</creatorcontrib><creatorcontrib>Rotkopf, Shay</creatorcontrib><creatorcontrib>Gabai, Rachel Malka</creatorcontrib><creatorcontrib>Zorde Khvalevsky, Elina</creatorcontrib><creatorcontrib>Muravnik, Sofia</creatorcontrib><creatorcontrib>Marzoli, Gabriela Alejandra</creatorcontrib><creatorcontrib>Domb, Abraham J.</creatorcontrib><creatorcontrib>Shemi, Amotz</creatorcontrib><creatorcontrib>Nyska, Abraham</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Toxicologic pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramot, Yuval</au><au>Rotkopf, Shay</au><au>Gabai, Rachel Malka</au><au>Zorde Khvalevsky, Elina</au><au>Muravnik, Sofia</au><au>Marzoli, Gabriela Alejandra</au><au>Domb, Abraham J.</au><au>Shemi, Amotz</au><au>Nyska, Abraham</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preclinical Safety Evaluation in Rats of a Polymeric Matrix Containing an siRNA Drug Used as a Local and Prolonged Delivery System for Pancreatic Cancer Therapy</atitle><jtitle>Toxicologic pathology</jtitle><addtitle>Toxicol Pathol</addtitle><date>2016-08-01</date><risdate>2016</risdate><volume>44</volume><issue>6</issue><spage>856</spage><epage>865</epage><pages>856-865</pages><issn>0192-6233</issn><eissn>1533-1601</eissn><abstract>Conventional chemotherapy treatments for pancreatic cancer are mainly palliative. RNA interference (RNAi)-based drugs present the potential for a new targeted treatment. LOcal Drug EluteR (LODERTM) is a novel biodegradable polymeric matrix that shields drugs against enzymatic degradation and releases small interfering RNA (siRNA) against G12D-mutated KRAS (siG12D). siG12D-LODER has successfully passed a phase 1/2a clinical trial. Such a formulation necessitates biocompatibility and safety studies. We describe the safety and toxicity studies with siG12D-LODER in 192 Hsd:Sprague Dawley rats, after repeated subcutaneous administrations (days 1, 14, and 28). Animals were sacrificed on days 29 and 42 (recovery phase). In all groups, no adverse effects were noted, and all animals showed favorable local and systemic tolerability. Histopathologically, LODER implantation resulted in the expected capsule formation, composed of a thin fibrotic tissue. 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subjects | Animals Antineoplastic Agents - pharmacology Carcinoma, Pancreatic Ductal - drug therapy Drug Carriers - pharmacology Lactic Acid - pharmacology Pancreatic Neoplasms - drug therapy Polyglycolic Acid - pharmacology Proto-Oncogene Proteins p21(ras) - antagonists & inhibitors Proto-Oncogene Proteins p21(ras) - genetics Rats Rats, Sprague-Dawley RNA, Small Interfering - pharmacology |
title | Preclinical Safety Evaluation in Rats of a Polymeric Matrix Containing an siRNA Drug Used as a Local and Prolonged Delivery System for Pancreatic Cancer Therapy |
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