Synthesis and Characterization of Dimeric Artesunate Glycerol Monocaprylate Conjugate and Formulation of Nanoemulsion Preconcentrate
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[1] V. K. Rai,et al. Opportunity in nanomedicine to counter the challenges of current drug delivery approaches used for the treatment of malaria: a review , 2023, Journal of drug targeting.
[2] N. Hasan,et al. Influence of Tacticity on the Structure Formation of Poly(methacrylic acid) in Langmuir/Langmuir−Blodgett and Thin Films , 2022, Macromolecular Chemistry and Physics.
[3] E. Wynendaele,et al. Degradation kinetics of artesunate for the development of an ex-tempore intravenous injection , 2022, Malaria journal.
[4] S. Parija. World Health Organization Day 2022 “Our Planet, Our Health” , 2022, Pondicherry Journal of Nursing.
[5] K. Mäder,et al. Controlled release starch-lipid implant for the therapy of severe malaria. , 2022, International journal of pharmaceutics.
[6] Xinsong Li,et al. Dimeric Artesunate Glycerophosphocholine Conjugate Nano-Assemblies as Slow-Release Antimalarials to Overcome Kelch 13 Mutant Artemisinin Resistance , 2022, Antimicrobial agents and chemotherapy.
[7] J. Kressler,et al. Microbial Transglutaminase-Mediated Formation of Erythropoietin-Polyester Conjugates. , 2022, Journal of biotechnology.
[8] S. Tsogoeva,et al. Artemisinin‐derived dimers from a chemical perspective , 2021, Medicinal research reviews.
[9] Pitambar Khanal. Antimalarial and anticancer properties of artesunate and other artemisinins: current development , 2021, Monatshefte für Chemie - Chemical Monthly.
[10] Omar Sarheed,et al. Studies on the Effect of Oil and Surfactant on the Formation of Alginate-Based O/W Lidocaine Nanocarriers Using Nanoemulsion Template , 2020, Pharmaceutics.
[11] D. Bonn,et al. Deposits from evaporating emulsion drops , 2020, Scientific Reports.
[12] Y. Tu,et al. The birth of artemisinin. , 2020, Pharmacology & therapeutics.
[13] S. Alven,et al. Nanoparticles Formulations of Artemisinin and Derivatives as Potential Therapeutics for the Treatment of Cancer, Leishmaniasis and Malaria , 2020, Pharmaceutics.
[14] E. Balogun,et al. Enhancing the antimalarial activity of artesunate , 2020, Parasitology Research.
[15] I. Rabinowitch,et al. Oral Administration of Artemisone for the Treatment of Schistosomiasis: Formulation Challenges and In Vivo Efficacy , 2020, Pharmaceutics.
[16] J. Sharifi‐Rad,et al. Medicinal plants used in the treatment of Malaria: A key emphasis to Artemisia, Cinchona, Cryptolepis, and Tabebuia genera , 2020, Phytotherapy research : PTR.
[17] S. Munnangi,et al. A vaginal nanoformulation of a SphK inhibitor attenuates lipopolysaccharide-induced preterm birth in mice. , 2019, Nanomedicine.
[18] Hari Prasad Devkota,et al. Bioactive Compounds and Health Benefits of Artemisia Species , 2019, Natural Product Communications.
[19] Celia N. Cruz,et al. Analytical considerations for measuring the globule size distribution of cyclosporine ophthalmic emulsions , 2018, International journal of pharmaceutics.
[20] Zhi-xiu Lin,et al. Self-nanoemulsifying drug delivery system of bruceine D: a new approach for anti-ulcerative colitis , 2018, International journal of nanomedicine.
[21] C. Yao,et al. Liposomes of dimeric artesunate phospholipid: A combination of dimerization and self-assembly to combat malaria. , 2018, Biomaterials.
[22] Amir Amani,et al. Design and evaluation of oral nanoemulsion drug delivery system of mebudipine , 2016, Drug delivery.
[23] S. Tsogoeva,et al. Artemisinin-Derived Dimers: Potent Antimalarial and Anticancer Agents. , 2016, Journal of medicinal chemistry.
[24] T. Efferth,et al. Highly potent artemisinin-derived dimers and trimers: Synthesis and evaluation of their antimalarial, antileukemia and antiviral activities. , 2015, Bioorganic & medicinal chemistry.
[25] D. Sullivan,et al. Antimalarial chemotherapy: orally curative artemisinin-derived trioxane dimer esters. , 2015, Bioorganic & medicinal chemistry letters.
[26] S. Mir,et al. Solid-Nanoemulsion Preconcentrate for Oral Delivery of Paclitaxel: Formulation Design, Biodistribution, and γ Scintigraphy Imaging , 2014, BioMed research international.
[27] Tingting Liu,et al. Nanoemulsion for Solubilization, Stabilization, and In Vitro Release of Pterostilbene for Oral Delivery , 2014, AAPS PharmSciTech.
[28] Philip Smith,et al. Synthesis, in vitro antiplasmodial activity and cytotoxicity of a series of artemisinin-triazine hybrids and hybrid-dimers. , 2014, European journal of medicinal chemistry.
[29] P. Vavia,et al. Medium chain triglyceride (MCT) rich, paclitaxel loaded self nanoemulsifying preconcentrate (PSNP): a safe and efficacious alternative to Taxol. , 2013, Journal of biomedical nanotechnology.
[30] D. Sullivan,et al. Synthesis and antimalarial efficacy of two-carbon-linked, artemisinin-derived trioxane dimers in combination with known antimalarial drugs. , 2013, Journal of medicinal chemistry.
[31] Lars Konermann,et al. Unraveling the mechanism of electrospray ionization. , 2013, Analytical chemistry.
[32] O. Abdallah,et al. Nanoemulsion liquid preconcentrates for raloxifene hydrochloride: optimization and in vivo appraisal , 2012, International journal of nanomedicine.
[33] Pharmaceutical Press,et al. Handbook of Pharmaceutical Excipients , 2012 .
[34] Y. Tu. The discovery of artemisinin (qinghaosu) and gifts from Chinese medicine , 2011, Nature Medicine.
[35] C. A. Morris,et al. Review of the clinical pharmacokinetics of artesunate and its active metabolite dihydroartemisinin following intravenous, intramuscular, oral or rectal administration , 2011, Malaria Journal.
[36] Y. Chevalier,et al. Microemulsion Microstructure Influences the Skin Delivery of an Hydrophilic Drug , 2011, Pharmaceutical Research.
[37] V. Barton,et al. The Molecular Mechanism of Action of Artemisinin—The Debate Continues , 2010, Molecules.
[38] P. G. Rao,et al. Artemisinin and its derivatives: a novel class of anti-malarial and anti-cancer agents. , 2010, Chemical Society reviews.
[39] M. Travassos,et al. Resistance to Antimalarial Drugs: Molecular, Pharmacologic, and Clinical Considerations , 2009, Pediatric Research.
[40] Andreas Briel,et al. Stabilization of indocyanine green by encapsulation within micellar systems. , 2009, Molecular pharmaceutics.
[41] R. Prud’homme,et al. Modulating the therapeutic activity of nanoparticle delivered paclitaxel by manipulating the hydrophobicity of prodrug conjugates. , 2008, Journal of medicinal chemistry.
[42] L. Chekem,et al. [Extraction of artemisinin and synthesis of its derivates artesunate and artemether]. , 2006, Medecine tropicale : revue du Corps de sante colonial.
[43] T. Tadros,et al. Formation and stability of nano-emulsions. , 2004, Advances in colloid and interface science.
[44] T. Shapiro,et al. Orally active, antimalarial, anticancer, artemisinin-derived trioxane dimers with high stability and efficacy. , 2003, Journal of medicinal chemistry.
[45] D. Mcclements. Colloidal basis of emulsion color , 2002 .
[46] D. Mcclements. Theoretical prediction of emulsion color. , 2002, Advances in colloid and interface science.
[47] M. Bockarie,et al. Apparent drug failure following artesunate treatment of Plasmodium falciparum malaria in Freetown, Sierra Leone: four case reports , 2001 .
[48] Bradley. Dimeric malarial drugs for enhanced activity. , 2000, Drug discovery today.
[49] T. Shapiro,et al. Antimalarial, antiproliferative, and antitumor activities of artemisinin-derived, chemically robust, trioxane dimers. , 1999, Journal of medicinal chemistry.
[50] W. Steglich,et al. Simple Method for the Esterification of Carboxylic Acids , 1978 .
[51] N. Boechat,et al. Current Antimalarial Therapies and Advances in the Development of Semi-Synthetic Artemisinin Derivatives. , 2018, Anais da Academia Brasileira de Ciencias.
[52] WHO calls for an immediate halt to provision of single-drug artemisinin malaria pills. New malaria treatment guidelines issued by WHO. , 2006, Saudi medical journal.