共 100 条
New insights into nanomedicines for oral delivery of glucagon-like peptide-1 analogs
被引:5
作者:

Pinto, Soraia Filipa Tavares
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机构:
Univ Porto, Inst Invest & Inovacao Saude I3S, Porto, Portugal
Univ Porto, Inst Ciencias Biomed Abel Salazar ICBAS, Porto, Portugal Univ Porto, Inst Invest & Inovacao Saude I3S, Porto, Portugal

Santos, Helder Almeida
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h-index: 0
机构:
Univ Helsinki, Fac Pharm, Drug Res Program, Div Pharmaceut Chem & Technol, Helsinki, Finland
Univ Groningen, Univ Med Ctr Groningen, WJ Kolff Inst Biomed Engn & Mat Sci, Groningen, Netherlands
Univ Groningen, Univ Med Ctr Groningen, Dept Biomed Engn, Groningen, Netherlands Univ Porto, Inst Invest & Inovacao Saude I3S, Porto, Portugal

Sarmento, Bruno Filipe Carmelino Cardoso
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h-index: 0
机构:
Univ Porto, Inst Invest & Inovacao Saude I3S, Porto, Portugal
CESPU, IUCS, Gandra, Portugal
Univ Porto, Inst Invest & Inovacao Saude I3S, Rua Alfredo Allen 208, P-4200135 Porto, Portugal Univ Porto, Inst Invest & Inovacao Saude I3S, Porto, Portugal
机构:
[1] Univ Porto, Inst Invest & Inovacao Saude I3S, Porto, Portugal
[2] Univ Porto, Inst Ciencias Biomed Abel Salazar ICBAS, Porto, Portugal
[3] Univ Helsinki, Fac Pharm, Drug Res Program, Div Pharmaceut Chem & Technol, Helsinki, Finland
[4] Univ Groningen, Univ Med Ctr Groningen, WJ Kolff Inst Biomed Engn & Mat Sci, Groningen, Netherlands
[5] Univ Groningen, Univ Med Ctr Groningen, Dept Biomed Engn, Groningen, Netherlands
[6] CESPU, IUCS, Gandra, Portugal
[7] Univ Porto, Inst Invest & Inovacao Saude I3S, Rua Alfredo Allen 208, P-4200135 Porto, Portugal
关键词:
antidiabetic peptides;
glucagon-like peptide-1;
nanocarriers;
oral delivery;
type 2 diabetes mellitus;
GLP-1 RECEPTOR AGONIST;
TYPE-2;
DIABETES-MELLITUS;
BETA-CELL FUNCTION;
POLYMERIC NANOPARTICLES;
DPP4;
INHIBITOR;
DRUG DELIVERY;
DUAL GIP;
EXENATIDE;
GLUCOSE;
SYSTEM;
D O I:
10.1002/wnan.1952
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Type 2 diabetes mellitus (T2DM) is a metabolic disorder that arises when the body cannot respond fully to insulin, leading to impaired glucose tolerance. Currently, the treatment embraces non-pharmacological actions (e.g., diet and exercise) co-associated with the administration of antidiabetic drugs. Metformin is the first-line treatment for T2DM; nevertheless, alternative therapeutic strategies involving glucagon-like peptide-1 (GLP-1) analogs have been explored for managing the disease. GLP-1 analogs trigger insulin secretion and suppress glucagon release in a glucose-dependent manner thereby, reducing the risk of hyperglycemia. Additionally, GLP-1 analogs have an extended plasma half-life compared to the endogenous peptide due to their high resistance to degradation by dipeptidyl peptidase-4. However, GLP-1 analogs are mainly administered via subcutaneous route, which can be inconvenient for the patients. Even considering an oral delivery approach, GLP-1 analogs are exposed to the harsh conditions of the gastrointestinal tract (GIT) and the intestinal barriers (mucus and epithelium). Hereupon, there is an unmet need to develop non-invasive oral transmucosal drug delivery strategies, such as the incorporation of GLP-1 analogs into nanoplatforms, to overcome the GIT barriers. Nanotechnology has the potential to shield antidiabetic peptides against the acidic pH and enzymatic activity of the stomach. In addition, the nanoparticles can be coated and/or surface-conjugated with mucodiffusive polymers and target intestinal ligands to improve their transport through the intestinal mucus and epithelium. This review focuses on the main hurdles associated with the oral administration of GLP-1 and GLP-1 analogs, and the nanosystems developed to improve the oral bioavailability of the antidiabetic peptides. This article is categorized under: Therapeutic Approaches and Drug Discovery > Nanomedicine for Infectious Disease Nanotechnology Approaches to Biology > Nanoscale Systems in Biology
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:9199-9207

Araujo, Francisca
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机构:
Univ Porto, INEB Inst Engn Biomed, P-4150180 Oporto, Portugal
Univ Porto, ICBAS, P-4050313 Oporto, Portugal
Univ Helsinki, Fac Pharm, Div Pharmaceut Chem & Technol, FI-00014 Helsinki, Finland Univ Porto, INEB Inst Engn Biomed, P-4150180 Oporto, Portugal

Shrestha, Neha
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机构:
Univ Helsinki, Fac Pharm, Div Pharmaceut Chem & Technol, FI-00014 Helsinki, Finland Univ Porto, INEB Inst Engn Biomed, P-4150180 Oporto, Portugal

Shahbazi, Mohammed-Ali
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机构:
Univ Helsinki, Fac Pharm, Div Pharmaceut Chem & Technol, FI-00014 Helsinki, Finland Univ Porto, INEB Inst Engn Biomed, P-4150180 Oporto, Portugal

Fonte, Pedro
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机构:
CESPU, Inst Super Ciencias Saude Norte, INFACTS Inst Invest Formacao Avancada Ciencias &, Dept Pharmaceut Sci, P-4585116 Gandra, Portugal
Univ Porto, Fac Pharm, REQUIMTE, Dept Chem Sci,Appl Chem Lab, P-4050313 Oporto, Portugal Univ Porto, INEB Inst Engn Biomed, P-4150180 Oporto, Portugal

Makila, Ermei M.
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机构:
Univ Helsinki, Fac Pharm, Div Pharmaceut Chem & Technol, FI-00014 Helsinki, Finland
Univ Turku, Dept Phys & Astron, Lab Ind Phys, FI-20014 Turku, Finland Univ Porto, INEB Inst Engn Biomed, P-4150180 Oporto, Portugal

Salonen, Jarno J.
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Univ Turku, Dept Phys & Astron, Lab Ind Phys, FI-20014 Turku, Finland Univ Porto, INEB Inst Engn Biomed, P-4150180 Oporto, Portugal

Hirvonen, Jouni T.
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机构:
Univ Helsinki, Fac Pharm, Div Pharmaceut Chem & Technol, FI-00014 Helsinki, Finland Univ Porto, INEB Inst Engn Biomed, P-4150180 Oporto, Portugal

Granja, Pedro L.
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机构:
Univ Porto, INEB Inst Engn Biomed, P-4150180 Oporto, Portugal
Univ Porto, ICBAS, P-4050313 Oporto, Portugal Univ Porto, INEB Inst Engn Biomed, P-4150180 Oporto, Portugal

Santos, Helder A.
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机构:
Univ Helsinki, Fac Pharm, Div Pharmaceut Chem & Technol, FI-00014 Helsinki, Finland Univ Porto, INEB Inst Engn Biomed, P-4150180 Oporto, Portugal

Sarmento, Bruno
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机构:
Univ Porto, INEB Inst Engn Biomed, P-4150180 Oporto, Portugal
CESPU, Inst Super Ciencias Saude Norte, INFACTS Inst Invest Formacao Avancada Ciencias &, Dept Pharmaceut Sci, P-4585116 Gandra, Portugal Univ Porto, INEB Inst Engn Biomed, P-4150180 Oporto, Portugal