Preparation and characterization of artemether loaded solid lipid nanoparticles: a 3² factorial design approach

References

• Ramteke KH, Joshi SA, Dhole SN. Solid lipid nanoparticle: a review. IOSR J Pharm. 2012;2:34–44.
   Google Scholar
• Garud A, Singh D, Garud N. Solid lipid nanoparticles (SLN): method, characterization and applications. Int Curr Pharm J. 2012;1:384–393.
   Google Scholar
• Song-Hong Z, Shen SC, Chen Z, et al. Preparation of solid lipid nanoparticles in co-flowing microchannels. Chem Eng J. 2008;144:324–328.
   Web of Science ®Google Scholar
• Mohd Y, Sara UVS. Preparation and optimization of haloperidol loaded solid lipid nanoparticles by Box–Behnken design. J Pharm Res. 2013;7:551–558.
   Google Scholar
• Durgaramani S, Madavan B, Penmatsa SD, et al. Formulation and characterization of solid lipid nanoparticles of rifampicin. Erciyes Med J. 2012;35:1–5.
   Google Scholar
• Ekambaram P, Sathali AAH, Priyanka K. Solid lipid nanoparticles: a review. Sci Revs Chem Commun. 2012;2:80–102.
   Web of Science ®Google Scholar
• Mohammad MM, Daneshamouz S, Samani SM, et al. A novel method to produce solid lipid nanoparticles using n-butanol as an additional co-surfactant according to the o/w microemulsion quenching technique. Chem Phys Lipids. 2013;174:32–38.
   PubMed Web of Science ®Google Scholar
• Bhandari R, Kaur IP. Pharmacokinetics, tissue distribution and relative bioavailability of isoniazid-solid lipid nanoparticles. Int J Pharm. 2013;441:202–212.
   PubMed Web of Science ®Google Scholar
• Bhandari R, Kaur IP. A method to prepare solid lipid nanoparticles with improved entrapment efficiency of hydrophilic drugs. Curr Nanosci. 2013;9:211–220.
   Web of Science ®Google Scholar
• Sharma V. Solid lipid nanoparticles system: an overview. Int J Res Pharm Sci. 2016;2:450–461.
   Google Scholar
• Negi J, Chattopadhyay P, Sharma A, et al. Development of solid lipid nanoparticles (SLNs) of lopinavir using hot self nano-emulsification (SNE) technique. Eur J Pharm Sci. 2013;48:231–239.
   PubMed Web of Science ®Google Scholar
• Zariwala MG, Elsaid N, Jackson TL, et al. A novel approach to oral iron delivery using ferrous sulphate loaded solid lipid nanoparticles. Int J Pharm. 2013;456:400–407.
   PubMed Web of Science ®Google Scholar
• Yuancai D, Wai KN, Shen S, et al. Solid lipid nanoparticles: continuous and potential large-scale nanoprecipitation production in static mixers. Colloids Surf B Biointerfaces. 2012;94:68–72.
   PubMed Web of Science ®Google Scholar
• Kamble MS, Vaidya KK, Bhosale AV, et al. Solid lipid nanoparticles and nanostructured lipid carriers–an overview. Int J Pharm Chem Biol Sci. 2012;4:681–691.
   Google Scholar
• Andrew L. Solid lipid nanoparticles for the delivery of pharmaceutical actives. Drug Deliv Technol. 2009;8:32–37.
   Google Scholar
• Pawar JN, Shete RT, Gangurde AB, et al. Development of amorphous dispersions of artemether with hydrophilic polymers via spray drying: physicochemical and in silico studies. Asian J Pharm Pharm Sci. 2016;11:385–395.
   Web of Science ®Google Scholar
• Mokale V, Rajput R, Patil J, et al. Formulation of metformin hydrochloride nanoparticles by using spray drying technique and in vitro evaluation of sustained release with 32-level factorial design approach. Drying Technol. 2016;34:1455–1461.
   Web of Science ®Google Scholar
• Verma U, Naik Jitendra B, Patil Jayesh S, et al. Screening of process variables to enhance the solubility of famotidine with 2-HydroxyPropyl–β-Cyclodextrin and PVP k30 by using Plackett–Burman design approach. Mat Sci Eng C. 2017;77:282–292.
   PubMed Web of Science ®Google Scholar
• Naik JB, Lokhande AB, Mishra S, et al. Development of sustained release micro/nanoparticles using different solvent emulsification technique: A review. Int J Pharm Bio Sci. 2012;4:573–590.
   Google Scholar
• Thakkar FMVT, Soni TG, Gohel MC. Supercritical fluid technology: a promising approach to enhance the drug solubility. Pharm Sci Res. 2009;1:1–14.
   Google Scholar
• Kuthuru S, Nangia A. Lornoxicam salts: crystal structures, conformations, and solubility. Cryst Growth Des. 2014;4:2945–2953.
   Google Scholar
• Moradiya HG, Islam MT, Halsey S, et al. Continuous co-crystallisation of carbamazepine and trans-cinnamic acid via melt extrusion processing. Cryst Eng Comm. 2014;16:3573–3583.
   Google Scholar
• Dolapo O, Jayawickrama D, Dongsheng B, et al. A control strategy for bioavailability enhancement by size reduction: effect of micronization conditions on the bulk, surface and blending characteristics of an active pharmaceutical ingredient. Powder Technol. 2014;258:222–233.
   Web of Science ®Google Scholar
• Onoue S, Terasawa N, Nakamura T, et al. Biopharmaceutical characterization of nanocrystalline solid dispersion of coenzyme Q 10 prepared with cold wet-milling system. Eur J Pharm Sci. 2014;53::118–125.
   PubMed Web of Science ®Google Scholar
• Megdi E, Bakhshi PK, Stride E, et al. Preparation of solid lipid nanoparticles containing active compound by electrohydrodynamic spraying. Food Res Int. 2013;53:88–95.
   Web of Science ®Google Scholar
• Schoenitz M, Joseph S, Nitz A, et al. Controlled polymorphic transformation of continuously crystallized solid lipid nanoparticles in a microstructured device: a feasibility study. Eur J Pharm Biopharm. 2014;86:324–331.
   PubMed Web of Science ®Google Scholar
• Yadava S, Naik JB, Patil JS, et al. Enhanced solubility and bioavailability of lovastatin using stabilized form of self-emulsifying drug delivery system. Colloids Surf A Physicochem Eng Asp. 2015;481:63–71.
   Web of Science ®Google Scholar
• Patil JS, Patil PB, Sonawane P, et al. Design and development of sustained-release glyburide-loaded silica nanoparticles. Bull Mater Sci. 2017;40:263–270.
   Web of Science ®Google Scholar
• Naik JB, Mokale VJ, Shevalkar GB, et al. Formulation and evaluation of poly (L-lactide-co-[epsilon]-caprolactone) loaded gliclazide biodegradable nanoparticles as a control release carrier. Int J Drug Deliv. 2013;5:300.
   Google Scholar
• Parshar D, Aditya NP, Murthy RSR. Development of artemether and lumefantrine co-loaded nanostructured lipid carriers: physicochemical characterization and in vivo antimalerial activity. Drug Deliv. 2016;23:123–129.
   PubMed Web of Science ®Google Scholar
• Ammar HO, Mahmoud MG, Mahmoud AA, et al. Formulation of risperidone in floating microparticles to alleviate its extrapyramidal side effects. Future ‎J Pharm Sci. 2016;2:43–59.
   Web of Science ®Google Scholar
• Ansari MT, Karim S, Ranjha NM, et al. Physicochemical characterization of artemether solid dispersions with hydrophilic carriers by freeze dried and melt method. Arch Pharm Res. 2010;33:901–910.
   PubMed Web of Science ®Google Scholar
• Deshmukh RK, Naik JB. Diclofenac sodium-loaded Eudragit® microspheres: optimization using statistical experimental design. J Pharm Innov. 2013;8:276–287.
   Web of Science ®Google Scholar
• Waghulde M, Naik JB. Comparative study of encapsulated vildagliptin microparticles produced by spray drying and solvent evaporation technique. Drying Technol. 2017;35:1645–1665.
   Web of Science ®Google Scholar
• Mokale VJ, Naik JB, Sutar Y, et al. Chitosan reinforced alginate controlled release beads of losartan potassium: design, formulation and in vitro evaluation. J Pharm Investig. 2014;44:243–252.
   Google Scholar
• Khairnar G, Naik JB, Mokale VJ. A statistical study on the development of micro particulate sustained drug delivery system for Losartan potassium by 32 factorial design approach. Bull Fac Pharm Cairo Univ. 2017;55:19–29.
   Google Scholar