pH Sensitive Complex Hydrogels for Protein Drug Release
pH Sensitive Complex Hydrogels for Protein Drug Release
批准号:
8619623
负责人:
Anthony M Lowman
金额:
$37.95万
依托单位国家:
美国
项目类别:
财政年份:
1989
资助国家:
美国
项目状态:
已结题
起止时间:
1989-12-01 至 2016-02-29
关键词:
AcidsAdhesivesAdvanced DevelopmentAgreementApplications GrantsAttentionBacterial AdhesinsBeliefBiological AvailabilityBlood CirculationCalcitoninCarbohydratesCarrier ProteinsCell modelComplexDevelopmentDrug Delivery SystemsDrug DesignDrug FormulationsDrug TransportEngineeringEnvironmentEpithelialEpithelial CellsEthylene GlycolsExhibitsGastrointestinal TransitGastrointestinal tract structureGelGlucoseGoalsGrantHydrogelsIn VitroInsulinIntestinal MucosaIntestinesIsoelectric PointLeadLegal patentLiquid substanceMembraneMethodologyMolecularNatureOralOral AdministrationPeptide HydrolasesPeptidesPharmaceutical PreparationsPhasePolymersPropertyProteinsPyrrolidinonesResearchResearch DesignResistanceRodent ModelRouteSeriesSimulateSmall IntestinesSolubilitySomatotropinStomachStructureSystemTestingTimeTransferrinUniversitiesVertebral columnWorkabsorptioncommercializationcompliance behaviorcontrolled releasecytotoxicitydiabetic ratenzyme activityethylene glycolgastrointestinalimprovedin vivomethacrylic acidmonolayernovelnovel strategiesnovel therapeuticspublic health relevanceresidencesuccesstherapeutic protein
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): This is a resubmission of a competing renewal proposal of grant RO1 EB000246-17 for the continuation of our studies on the fundamental understanding of transmucosal delivery of drugs, peptides and proteins using a series of novel biopolymeric complexation carriers with unique properties and in advanced controlled release systems. It has generally been believed that peptides and proteins such as insulin cannot be administered via the oral route because of their degradation by the proteolytic enzymes in the gastrointestinal tract and their extremely slow rate of transport across the mucosal membrane. A successful oral delivery system for protein drugs could lead to the development of new therapeutics with increased patient compliance and efficacy. Our group has developed a new class of polymeric complexation hydrogels comprised of poly (ethylene glycol) (PEG) chains grafted on poly (methacrylic acid) (PMAA) backbone chain. The new systems, henceforth designated as P (MAA-g-EG), have shown extreme promise as oral delivery vehicles for insulin, calcitonin, and growth hormone. Prior studies have established that these systems are promising candidates for oral delivery of insulin. Yet, our more recent work and attention is now focused on continued strategies for enhancing the bioavailability of oral delivered proteins, in addition to insulin. The methodologies we intend to pursue in this competing renewal proposal include: (i) developing further strategies for protection of the protein in the GI lumen; (ii) enhancing transport of the proteins across the GI lumen; and (iii) increasing the residence times in the upper small intestine through enhanced bioadhesion. While some strategies have been previously investigated with moderate success using insulin, in this work, we will pursue novel strategies that may provide significant advances over our prior studies with insulin. Additionally, we intend to further develop these complexation hydrogels for oral delivery of other therapeutic proteins such as calcitonin and growth hormone.
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DOI:
10.1002/adma.201303233
发表时间:
2014-01-08
期刊:
ADVANCED MATERIALS
影响因子:
29.4
作者:
[Annabi, Nasim, Tamayol, Ali, Uquillas, Jorge Alfredo, Akbari, Mohsen, Bertassoni, Luiz E., Cha, Chaenyung, Camci-Unal, Gulden, Dokmeci, Mehmet R., Peppas, Nicholas A., Khademhosseini, Ali]
通讯作者:
Khademhosseini, Ali
DOI:
10.1021/bm500588x
发表时间:
2014-07-14
期刊:
Biomacromolecules
影响因子:
6.2
作者:
[Durán-Lobato M, Carrillo-Conde B, Khairandish Y, Peppas NA]
通讯作者:
Peppas NA
DOI:
10.1021/ie201593h
发表时间:
2011-11-16
期刊:
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
影响因子:
4.2
作者:
[Schoener, Cody A., Hutson, Heather N., Fletcher, Grace K., Peppas, Nicholas A.]
通讯作者:
Peppas, Nicholas A.
Effectiveness of Intravenous Infusion Algorithms for Glucose Control in Diabetic Patients Using Different Simulation Models.
使用不同的模拟模型,静脉输注算法对糖尿病患者的葡萄糖控制的有效性。
DOI:
10.1021/ie800871t
发表时间:
2009-03-24
期刊:
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
影响因子:
4.2
作者:
[Farmer, Terry G., Jr., Edgar, Thomas F., Peppas, Nicholas A.]
通讯作者:
Peppas, Nicholas A.
DOI:
10.1146/annurev-chembioeng-073009-100847
发表时间:
2010
期刊:
Annual review of chemical and biomolecular engineering
影响因子:
8.4
作者:
[Liechty WB, Kryscio DR, Slaughter BV, Peppas NA]
通讯作者:
Peppas NA
共 46 条
Engineering a multifunctional injectable scaffold for spinal cord repair
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批准号:7589538
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项目类别:
-
资助金额:$16.41万
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财政年份:2008
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负责人:Anthony M Lowman
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依托单位:
pH Sensitive Complex Hydrogels for Protein Drug Release
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批准号:8234865
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项目类别:
-
资助金额:$39.6万
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财政年份:1989
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负责人:Anthony M Lowman
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依托单位:
pH Sensitive Complex Hydrogels for Protein Drug Release
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批准号:8433421
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项目类别:
-
资助金额:$37.12万
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财政年份:1989
-
负责人:Anthony M Lowman
-
依托单位:
pH Sensitive Complex Hydrogels for Protein Drug Release
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批准号:8107830
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项目类别:
-
资助金额:$45.21万
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财政年份:1989
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负责人:Anthony M Lowman
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依托单位:
海外基金