Advancements in nanotherapeutics for Alzheimer’s disease: current perspectives
Objectives Considerable progress has been made in the treatment of Alzheimer’s disease (AD), but all available strategies focus on alleviating symptoms rather than curing, which means that AD is viewed as an unresolvable neurodegenerative disease. Nanotechnological applications offer an alternative...
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Veröffentlicht in: | Journal of pharmacy and pharmacology 2019-09, Vol.71 (9), p.1370-1383 |
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description | Objectives Considerable progress has been made in the treatment of Alzheimer’s disease (AD), but all available strategies focus on alleviating symptoms rather than curing, which means that AD is viewed as an unresolvable neurodegenerative disease. Nanotechnological applications offer an alternative platform for the treatment of neurodegenerative diseases. This review aims to summarize the recent nanomedicine and nanotechnology developments for the treatment of AD. Key findings A plethora of nanocarriers and nanoparticle prodrugs have been reported to have negligible cytotoxicity in animal models, and these developments have revealed new opportunities for development of new classes of potent drug formulations for AD. Different nanotechnology‐based approaches such as polymers, emulsions, lipo‐carriers, solid lipid carriers, carbon nanotubes and metal‐based carriers have been developed over the past decade, and they have been focusing on both neuroprotective and neurogenerative techniques to treat AD. Studies also reveal that nanotechnological approaches can aid in early diagnosis of AD and enhance therapeutic efficacy and bioavailability. Summary Notably, the drugs used conventionally to target the central nervous system have limitations that include an inability to cross the ‘blood–brain barrier’ or the ‘blood–cerebrospinal fluid barrier’ effectively and high drug efflux due to the activity of P‐glycoprotein, but these limitations can be successfully overcome when nanocarriers are used for targeted drug delivery in AD. |
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Sahab ; Kim, Hoon ; Mathew, Bijo</creator><creatorcontrib>Harilal, Seetha ; Jose, Jobin ; Parambi, Della Grace Thomas ; Kumar, Rajesh ; Mathew, Githa Elizabeth ; Uddin, Md. Sahab ; Kim, Hoon ; Mathew, Bijo</creatorcontrib><description>Objectives Considerable progress has been made in the treatment of Alzheimer’s disease (AD), but all available strategies focus on alleviating symptoms rather than curing, which means that AD is viewed as an unresolvable neurodegenerative disease. Nanotechnological applications offer an alternative platform for the treatment of neurodegenerative diseases. This review aims to summarize the recent nanomedicine and nanotechnology developments for the treatment of AD. Key findings A plethora of nanocarriers and nanoparticle prodrugs have been reported to have negligible cytotoxicity in animal models, and these developments have revealed new opportunities for development of new classes of potent drug formulations for AD. Different nanotechnology‐based approaches such as polymers, emulsions, lipo‐carriers, solid lipid carriers, carbon nanotubes and metal‐based carriers have been developed over the past decade, and they have been focusing on both neuroprotective and neurogenerative techniques to treat AD. Studies also reveal that nanotechnological approaches can aid in early diagnosis of AD and enhance therapeutic efficacy and bioavailability. Summary Notably, the drugs used conventionally to target the central nervous system have limitations that include an inability to cross the ‘blood–brain barrier’ or the ‘blood–cerebrospinal fluid barrier’ effectively and high drug efflux due to the activity of P‐glycoprotein, but these limitations can be successfully overcome when nanocarriers are used for targeted drug delivery in AD.</description><identifier>ISSN: 0022-3573</identifier><identifier>EISSN: 2042-7158</identifier><identifier>DOI: 10.1111/jphp.13132</identifier><identifier>PMID: 31304982</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Alzheimer Disease - drug therapy ; Alzheimer Disease - physiopathology ; Alzheimer's disease ; Animal models ; Animals ; Bioavailability ; Biological Availability ; Blood ; Blood-Brain Barrier - drug effects ; blood–brain barrier ; Central nervous system ; Cerebrospinal fluid ; Chemical compounds ; Cholinesterase Inhibitors - chemistry ; Cholinesterase Inhibitors - therapeutic use ; Cytotoxicity ; Drug Carriers - therapeutic use ; Drug delivery ; Drug Delivery Systems - methods ; Emulsions ; Formulations ; Humans ; Lipids ; Medical treatment ; nanomedicine ; Nanomedicine - methods ; Nanoparticles ; Nanoparticles - therapeutic use ; Nanotechnology ; Nanotechnology - methods ; Nanotubes ; Nanotubes, Carbon ; Neurodegenerative diseases ; Neuroprotection ; Polymers ; Polymers - therapeutic use ; Prodrugs ; Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors</subject><ispartof>Journal of pharmacy and pharmacology, 2019-09, Vol.71 (9), p.1370-1383</ispartof><rights>2019 Royal Pharmaceutical Society</rights><rights>2019 Royal Pharmaceutical Society.</rights><rights>Copyright © 2019 Royal Pharmaceutical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3932-24de891edb7dd3598fea4236eb60aa2abc8d3361063c454b6c6893f432a74ec13</citedby><cites>FETCH-LOGICAL-c3932-24de891edb7dd3598fea4236eb60aa2abc8d3361063c454b6c6893f432a74ec13</cites><orcidid>0000-0002-6658-4497</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjphp.13132$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjphp.13132$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31304982$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Harilal, Seetha</creatorcontrib><creatorcontrib>Jose, Jobin</creatorcontrib><creatorcontrib>Parambi, Della Grace Thomas</creatorcontrib><creatorcontrib>Kumar, Rajesh</creatorcontrib><creatorcontrib>Mathew, Githa Elizabeth</creatorcontrib><creatorcontrib>Uddin, Md. Sahab</creatorcontrib><creatorcontrib>Kim, Hoon</creatorcontrib><creatorcontrib>Mathew, Bijo</creatorcontrib><title>Advancements in nanotherapeutics for Alzheimer’s disease: current perspectives</title><title>Journal of pharmacy and pharmacology</title><addtitle>J Pharm Pharmacol</addtitle><description>Objectives Considerable progress has been made in the treatment of Alzheimer’s disease (AD), but all available strategies focus on alleviating symptoms rather than curing, which means that AD is viewed as an unresolvable neurodegenerative disease. Nanotechnological applications offer an alternative platform for the treatment of neurodegenerative diseases. This review aims to summarize the recent nanomedicine and nanotechnology developments for the treatment of AD. Key findings A plethora of nanocarriers and nanoparticle prodrugs have been reported to have negligible cytotoxicity in animal models, and these developments have revealed new opportunities for development of new classes of potent drug formulations for AD. Different nanotechnology‐based approaches such as polymers, emulsions, lipo‐carriers, solid lipid carriers, carbon nanotubes and metal‐based carriers have been developed over the past decade, and they have been focusing on both neuroprotective and neurogenerative techniques to treat AD. Studies also reveal that nanotechnological approaches can aid in early diagnosis of AD and enhance therapeutic efficacy and bioavailability. Summary Notably, the drugs used conventionally to target the central nervous system have limitations that include an inability to cross the ‘blood–brain barrier’ or the ‘blood–cerebrospinal fluid barrier’ effectively and high drug efflux due to the activity of P‐glycoprotein, but these limitations can be successfully overcome when nanocarriers are used for targeted drug delivery in AD.</description><subject>Alzheimer Disease - drug therapy</subject><subject>Alzheimer Disease - physiopathology</subject><subject>Alzheimer's disease</subject><subject>Animal models</subject><subject>Animals</subject><subject>Bioavailability</subject><subject>Biological Availability</subject><subject>Blood</subject><subject>Blood-Brain Barrier - drug effects</subject><subject>blood–brain barrier</subject><subject>Central nervous system</subject><subject>Cerebrospinal fluid</subject><subject>Chemical compounds</subject><subject>Cholinesterase Inhibitors - chemistry</subject><subject>Cholinesterase Inhibitors - therapeutic use</subject><subject>Cytotoxicity</subject><subject>Drug Carriers - therapeutic use</subject><subject>Drug delivery</subject><subject>Drug Delivery Systems - methods</subject><subject>Emulsions</subject><subject>Formulations</subject><subject>Humans</subject><subject>Lipids</subject><subject>Medical treatment</subject><subject>nanomedicine</subject><subject>Nanomedicine - methods</subject><subject>Nanoparticles</subject><subject>Nanoparticles - therapeutic use</subject><subject>Nanotechnology</subject><subject>Nanotechnology - methods</subject><subject>Nanotubes</subject><subject>Nanotubes, Carbon</subject><subject>Neurodegenerative diseases</subject><subject>Neuroprotection</subject><subject>Polymers</subject><subject>Polymers - therapeutic use</subject><subject>Prodrugs</subject><subject>Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors</subject><issn>0022-3573</issn><issn>2042-7158</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90MtKw0AUBuBBFFurGx9AAm5ESJ1bJom7UtQqBbvQdZhMTuiU3JxJKnXla_h6PolTU1248GzO5js_hx-hU4LHxM3Vqlk2Y8IIo3toSDGnfkiCaB8NMabUZ0HIBujI2hXGOBRCHKKBs5jHER2ixSRby0pBCVVrPV15lazqdglGNtC1Wlkvr403Kd6WoEswn-8f1su0BWnh2lOdMe7Oa8DYBlSr12CP0UEuCwsnuz1Cz7c3T9OZP3-8u59O5r5iMaM-5RlEMYEsDbOMBXGUg-SUCUgFlpLKVEUZY4JgwRQPeCqUiGKWc0ZlyEERNkIXfW5j6pcObJuU2iooCllB3dmE0iAigosgdvT8D13Vnancd06JUJCA89Cpy14pU1trIE8ao0tpNgnBybbnZNtz8t2zw2e7yC4tIfulP8U6QHrwqgvY_BOVPCxmiz70C5rTiSM</recordid><startdate>201909</startdate><enddate>201909</enddate><creator>Harilal, Seetha</creator><creator>Jose, Jobin</creator><creator>Parambi, Della Grace Thomas</creator><creator>Kumar, Rajesh</creator><creator>Mathew, Githa Elizabeth</creator><creator>Uddin, Md. Sahab</creator><creator>Kim, Hoon</creator><creator>Mathew, Bijo</creator><general>Wiley Subscription Services, Inc</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>7QP</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6658-4497</orcidid></search><sort><creationdate>201909</creationdate><title>Advancements in nanotherapeutics for Alzheimer’s disease: current perspectives</title><author>Harilal, Seetha ; Jose, Jobin ; Parambi, Della Grace Thomas ; Kumar, Rajesh ; Mathew, Githa Elizabeth ; Uddin, Md. Sahab ; Kim, Hoon ; Mathew, Bijo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3932-24de891edb7dd3598fea4236eb60aa2abc8d3361063c454b6c6893f432a74ec13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Alzheimer Disease - drug therapy</topic><topic>Alzheimer Disease - physiopathology</topic><topic>Alzheimer's disease</topic><topic>Animal models</topic><topic>Animals</topic><topic>Bioavailability</topic><topic>Biological Availability</topic><topic>Blood</topic><topic>Blood-Brain Barrier - drug effects</topic><topic>blood–brain barrier</topic><topic>Central nervous system</topic><topic>Cerebrospinal fluid</topic><topic>Chemical compounds</topic><topic>Cholinesterase Inhibitors - chemistry</topic><topic>Cholinesterase Inhibitors - therapeutic use</topic><topic>Cytotoxicity</topic><topic>Drug Carriers - therapeutic use</topic><topic>Drug delivery</topic><topic>Drug Delivery Systems - methods</topic><topic>Emulsions</topic><topic>Formulations</topic><topic>Humans</topic><topic>Lipids</topic><topic>Medical treatment</topic><topic>nanomedicine</topic><topic>Nanomedicine - methods</topic><topic>Nanoparticles</topic><topic>Nanoparticles - therapeutic use</topic><topic>Nanotechnology</topic><topic>Nanotechnology - methods</topic><topic>Nanotubes</topic><topic>Nanotubes, Carbon</topic><topic>Neurodegenerative diseases</topic><topic>Neuroprotection</topic><topic>Polymers</topic><topic>Polymers - therapeutic use</topic><topic>Prodrugs</topic><topic>Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harilal, Seetha</creatorcontrib><creatorcontrib>Jose, Jobin</creatorcontrib><creatorcontrib>Parambi, Della Grace Thomas</creatorcontrib><creatorcontrib>Kumar, Rajesh</creatorcontrib><creatorcontrib>Mathew, Githa Elizabeth</creatorcontrib><creatorcontrib>Uddin, Md. Sahab</creatorcontrib><creatorcontrib>Kim, Hoon</creatorcontrib><creatorcontrib>Mathew, Bijo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmacy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harilal, Seetha</au><au>Jose, Jobin</au><au>Parambi, Della Grace Thomas</au><au>Kumar, Rajesh</au><au>Mathew, Githa Elizabeth</au><au>Uddin, Md. Sahab</au><au>Kim, Hoon</au><au>Mathew, Bijo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Advancements in nanotherapeutics for Alzheimer’s disease: current perspectives</atitle><jtitle>Journal of pharmacy and pharmacology</jtitle><addtitle>J Pharm Pharmacol</addtitle><date>2019-09</date><risdate>2019</risdate><volume>71</volume><issue>9</issue><spage>1370</spage><epage>1383</epage><pages>1370-1383</pages><issn>0022-3573</issn><eissn>2042-7158</eissn><abstract>Objectives Considerable progress has been made in the treatment of Alzheimer’s disease (AD), but all available strategies focus on alleviating symptoms rather than curing, which means that AD is viewed as an unresolvable neurodegenerative disease. Nanotechnological applications offer an alternative platform for the treatment of neurodegenerative diseases. This review aims to summarize the recent nanomedicine and nanotechnology developments for the treatment of AD. Key findings A plethora of nanocarriers and nanoparticle prodrugs have been reported to have negligible cytotoxicity in animal models, and these developments have revealed new opportunities for development of new classes of potent drug formulations for AD. Different nanotechnology‐based approaches such as polymers, emulsions, lipo‐carriers, solid lipid carriers, carbon nanotubes and metal‐based carriers have been developed over the past decade, and they have been focusing on both neuroprotective and neurogenerative techniques to treat AD. Studies also reveal that nanotechnological approaches can aid in early diagnosis of AD and enhance therapeutic efficacy and bioavailability. Summary Notably, the drugs used conventionally to target the central nervous system have limitations that include an inability to cross the ‘blood–brain barrier’ or the ‘blood–cerebrospinal fluid barrier’ effectively and high drug efflux due to the activity of P‐glycoprotein, but these limitations can be successfully overcome when nanocarriers are used for targeted drug delivery in AD.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31304982</pmid><doi>10.1111/jphp.13132</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-6658-4497</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alzheimer Disease - drug therapy Alzheimer Disease - physiopathology Alzheimer's disease Animal models Animals Bioavailability Biological Availability Blood Blood-Brain Barrier - drug effects blood–brain barrier Central nervous system Cerebrospinal fluid Chemical compounds Cholinesterase Inhibitors - chemistry Cholinesterase Inhibitors - therapeutic use Cytotoxicity Drug Carriers - therapeutic use Drug delivery Drug Delivery Systems - methods Emulsions Formulations Humans Lipids Medical treatment nanomedicine Nanomedicine - methods Nanoparticles Nanoparticles - therapeutic use Nanotechnology Nanotechnology - methods Nanotubes Nanotubes, Carbon Neurodegenerative diseases Neuroprotection Polymers Polymers - therapeutic use Prodrugs Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors |
title | Advancements in nanotherapeutics for Alzheimer’s disease: current perspectives |
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