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Advances in oral peptide drug nanoparticles for diabetes mellitus treatment 被引量:6

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摘要 Peptide drugs play an important role in diabetes mellitus treatment.Oral administration of peptide drugs is a promising strategy for diabetes mellitus because of its convenience and high patient compliance compared to parenteral administration routes.However,there are a series of formidable unfavorable conditions present in the gastrointestinal(GI)tract after oral administration,which result in the low oral bioavailability of these peptide drugs.To overcome these challenges,various nanoparticles(NPs)have been developed to improve the oral absorption of peptide drugs due to their unique in vivo properties and high design flexibility.This review discusses the unfavorable conditions present in the GI tract and provides the corresponding strategies to overcome these challenges.The review provides a comprehensive overview on the NPs that have been constructed for oral peptide drug delivery in diabetes mellitus treatment.Finally,we will discuss the rational application and give some suggestions that can be utilized for the development of oral peptide drug NPs.Our aim is to provide a systemic and comprehensive review of oral peptide drug NPs that can overcome the challenges in GI tract for efficient treatment of diabetes mellitus.
出处 《Bioactive Materials》 SCIE 2022年第9期392-408,共17页 生物活性材料(英文)
基金 supported by the National Natural Science Foundation of China(32071391,21905283,31771095,21875254,52073287 and 22075289) the Fundamental Research Funds for the Central Universities(06500230) the Beijing Nova Program(Z201100006820140).
作者简介 Corresponding author:Xin Zhang,xzhang@ipe.ac.cn;Corresponding author:Yan Li,E-mail addresses:liyan310@ustb.edu.cn。
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  • 1[1]Dieterle C,Brendel MD,Seissler J,Eckhard M,Bretzel RG,Landgraf R.[Therapy of diabetes mellitus.Pancreas transplantation,islet transplantation,stem cell and gene therapy] Internist (Bed) 2006; 47:489-496,498-501
  • 2[2]Samson SL,Chan L.Gene therapy for diabetes:reinventing the islet.Trends Endocrinol Metab 2006; 17:92-100
  • 3[3]Shapiro AM,Lakey JR,Ryan EA,Korbutt GS,Toth E,Warnock GL,Kneteman NM,Rajotte RV.Islet transplantation in seven patients with type 1 diabetes mellitus using a glucocorticoid-free immunosuppressive regimen.N Engl J Med 2000; 343:230-238
  • 4[4]Lau J,Mattsson G,Carlsson C,Nyqvist D,Kohler M,Berggren PO,Jansson L,Carlsson PO.Implantation sitedependent dysfunction of transplanted pancreatic islets.Diabetes 2007; 56:1544-1550
  • 5[5]Li M,Inaba M,Guo KQ,Hisha H,Abraham NG,Ikehara S.Treatment of streptozotocin-induced diabetes mellitus in mice by intra-bone marrow bone marrow transplantation plus portal vein injection of beta cells induced from bone marrow cells.Int J Hematol 2007; 86:438-445
  • 6[6]-9 Brenner S,Ryser MF,Whiting-Theobald NL,Gentsch M,Linton GF,Malech HL.The late dividing population of gamma-retroviral vector transduced human mobilized peripheral blood progenitor cells contributes most to genemarked cell engraftment in nonobese diabetic/severe combined immunodeficient mice.Stem Cells 2007; 25:1807-1813
  • 7[10]Timper K,Seboek D,Eberhardt M,Linscheid P,Christ Crain M,Keller U,Muller B,Zulewski H.Human adipose tissue-derived mesenchymal stem cells differentiate into insulin,somatostatin,and glucagon expressing cells.Biochem Biophys Res Commun 2006; 341:1135-1140
  • 8[11]Fukushima M,Hattori Y,Tsukada H,Koga K,Kajiwara E,Kawano K,Kobayashi T,Kamata K,Maitani Y.Adiponectin gene therapy of streptozotocin-induced diabetic mice using hydrodynamic injection.J Gene Med 2007; 9:976-985
  • 9[12]Yoo HS,Mazda O,Lee HY,Kim JC,Kwon SM,Lee JE,Kwon IC,Jeong H,Jeong YS,Jeong SY.In vivo gene therapy of type I diabetic mellitus using a cationic emulsion containing an Epstein Barr Virus (EBV) based plasmid vector.J Control Release 2006; 112:139-144
  • 10[13]Lu YC,Sternini C,Rozengurt E,Zhukova E.Release of transgenic human insulin from gastric g cells:a novel approach for the amelioration of diabetes.Endocrinology 2005; 146:2610-2619

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