Evaluation of dika wax-soybean oil-based artesunate-loaded lipospheres: in vitro–in vivo correlation studies

References

• Attama AA, Muller-Goymann CC. A critical study of novel physically structured lipid matrices composed of a homolipid from Capra hircus and theobroma oil. Int J Pharm, 2006;322:67–78
   PubMed Web of Science ®Google Scholar
• Attama AA, Muller-Goymann CC. Investigation of surface-modified solid lipid nanocontainers formulated with a heterolipid-templated homolipid. Int J Pharm, 2007;334:179–89
   PubMed Web of Science ®Google Scholar
• Attama AA, Nkemnele MO. In vitro evaluation of drug release from self micro-emulsifying drug delivery systems using a biodegradable homolipid from Capra hircus. Int J Pharm, 2005;304:4–10
   PubMed Web of Science ®Google Scholar
• Attama AA, Okafor CE, Builders PF, Okorie O. Formulation and in vitro evaluation of a PEGylated microscopic lipospheres delivery system for ceftriaxone sodium. Drug Deliv, 2009;16:448–616
   PubMed Web of Science ®Google Scholar
• Attama AA, Schicke BC, Müller-Goymann CC. Further characterization of theobroma oil beeswax admixtures as lipid matrices for improved drug delivery systems. Eur J Pharm Biopharm, 2006;64:294–306
   PubMed Web of Science ®Google Scholar
• Bloland P. 2001. Drug resistance in malaria. WHO monograph WHO/CDS/CSR/DRS/2001.4. Geneva: World Health Organization
   Google Scholar
• Brown SA, Chime SA, Attama AA, Agu C, Onunkwo GC. In vitro and in vivo characterisation of piroxicam-loaded dika wax lipospheres. Trop J Pharm Res, 2013;12(1):33–8
   Web of Science ®Google Scholar
• Chime SA, Attama AA, Agubata CO, Ogbonna JD, Onunkwo GC. Recent advances in lipospheres drug delivery system. J Pharm Res, 2012a;5(3):1743–8
   Google Scholar
• Chime SA, Attama AA, Obitte NC, Kenechukwu FC, Agubata CO, Ezekwe CC. In vitro and in vivo characterisation of indomethacin-loaded dika fat based solid lipid microparticles. Int J Pharm Rev Res, 2012b;16(2):10–16
   Google Scholar
• Chime SA, Attama AA, Builders PF, Onunkwo GC. Sustained release diclofenac potassium-loaded solid lipid microparticle, based on solidified reverse micellar solution (SRMS): In vitro and in vivo evaluation. J Microencapsul, 2013a;30(4):335–45
   PubMed Web of Science ®Google Scholar
• Chime SA, Onunkwo GC, Onyishi IV. Kinetics and mechanisms of drug release from swellable and non swellable matrices: A review. Res J Pharm Bio Chem Soc, 2013b;4(2):97–103
   Google Scholar
• Domb AJ, Manier M. Lipospheres for controlled delivery of Pharmaceuticals, pesticides, fertilizers. Nova pharmaceuticals, pesticides, fertilizers. Nova Pharmaceutical Corporation 90 - US 6519 (9107171), 1990;79:8–11
   Google Scholar
• El-Kamel HA, Al-Fagih MI, Alsarra AI. Testosterone solid lipid microparticles for transdermal drug delivery formulation and physicochemical characterisation. J Microencapsul, 2007;24(5):457–75
   PubMed Web of Science ®Google Scholar
• Fonollosa J, Camposa L, Marti M, de la Maza A, Parra JL, Coderch L. X-ray diffraction analysis of internal wool lipids. Chem Phys Lipids, 2004;130:159–66
   PubMed Web of Science ®Google Scholar
• Freitas C, Müller RH. Correlation between long-term stability of solid lipid nanoparticles (SLN) and crystallinity of the lipid phase. Eur J Pharm Biopharm, 1999;47:125–32
   PubMed Web of Science ®Google Scholar
• Gao P, Guyton ME, Huang T, Bauer JM, Stefanski KJ, Lu Q. Enhanced oral bioavailability of a poorly water soluble drug PNU-91325 by supersaturable formulations. Drug Dev Ind Pharm, 2004;30:221–9
   PubMed Web of Science ®Google Scholar
• Gupta V, Singla N. Antimalarial agents: The present concept. J Parasit Dis, 2007;21:1280–2
   Google Scholar
• Higuchi T. Mechanism of sustained-action medication. Theoretical analysis of rate of release of solid drugs dispersed in solid matrices. J Pharm Sci, 1963;52:1145–9
   PubMed Web of Science ®Google Scholar
• Hou DZ, Xie CS, Huang K, Zhu CH. The production and characteristics of solid lipid nanoparticles (SLN). Biomaterials, 2003;24:1781–5
   PubMed Web of Science ®Google Scholar
• Jaspart S, Piel G, Delatte L, Evrad B. Solid lipid microparticles: Formulation, preparation, characterization, drug release and applications. Expert Opin Drug Deliv, 2005;2:75–87
   PubMedGoogle Scholar
• Joshi NH, Shah N. Review of lipids in drug delivery systems – Part I. Am Pharm Rev, 2005;8:70–8
   Google Scholar
• Khopade AJ, Jain NK. Long circulating lipospheres targeted to inflamed tissue. Pharmazie, 1997;52:165–6
   PubMed Web of Science ®Google Scholar
• Kumar N. A vaccine to prevent transmission of human malaria: A long way to travel on a dusty and often bumpy road. Curr Sci, 2007;92:1535–44
   Web of Science ®Google Scholar
• Li Q, Weina P. Artesunate: The best drug in the treatment of severe and complicated malaria. Pharmaceuticals, 2010;3:2322–32
   Google Scholar
• Lindegardh N, Hampithakong W, Kamanikom B, Singhasivanon P, Socheat D, Yi P, Dondorp AM, McGready R, Nosten F, White NJ, Day NPJ. Major pitfalls in the measurement of artemisinin derivatives in plasma in clinical studies. J Chromatogr B, 2008;876:54–60
   PubMed Web of Science ®Google Scholar
• Liu K. 1999. Soybean: Chemistry, technology, and utilization. New York: Aspen Publishers, Inc
   Google Scholar
• Matos L, Nzikou JM, Pandzou-Yembe VN, Mapepoulou TG, Linder M, Desobrg S. Studies of Irvingia gabonensis seed kernels: Oil technological applications. Pak J Nutri, 2009;8(2):151–7
   Google Scholar
• Meara ML, Patel CB. The components acids and glycerides of dika wax. J Agric Food, 2006;12:40–57
   Google Scholar
• Moghimi HR, Williams AC, Barry BW. A lamellar matrix model for stratum corneum intercellular lipids. I. Characterization and comparison with stratum corneum intercellular structure. Int J Pharm, 1996;131:103–15
   Web of Science ®Google Scholar
• Nattee S, Natalie D. Eddington. In vitro/in vivo correlation definitions and regulatory guidance. Inter J Gen Drugs. Availabel at: http://www.locumusa.com. Accessed 3 May 2012
   Google Scholar
• Obitte NC, Chime SA, Magaret AA, Attama AA, Onyishi IV, Brown SA. Some in vitro and pharmacodynamic evaluation of indomethacin solid lipid microparticles. Afr J Pharm Pharmacol, 2012;6(30):2309–17
   Google Scholar
• Ofoefule SI, Chukwu A, Okore VC, Ugwah MO. Use of dika fat in the formulation of sustained release frusemide encapsulated granules. Boll Chim Farm, 1997;136(10):646–50
   PubMedGoogle Scholar
• Okorie VC. Effect of dika fat content of a barrier film coating on the kinetics of drug release from swelling polymeric systems. Boll Chim Farm, 2000;139(1):21–5
   PubMedGoogle Scholar
• Pouton CW. Lipid formulations for oral administration of drugs: Non emulsifying, self-emulsifying and self micro emulsifying drug delivery systems. Eur J Pharm Sci, 2000;11:93–8
   Google Scholar
• Rawat SM, Singh D, Saraf S. Formulation optimization of controlled delivery systems for antihypertensive peptides using response surface methodology. Amer J Drug Dis Dev, 2011;1(3):174–87
   Google Scholar
• Ritger PL, Peppas NA. A simple equation for description of solute release 1. Fickian and non-Fickian release from non swellable device in the form of slabs, spheres, cylinders and discs. J Control Release, 1987;5:23–36
   Google Scholar
• Sanna V, Kirschvink N, Gustin P, Gavini E, Roland I, Delattera L, Evrad B. Preparation and in vivo toxicity study of solid lipid microparticles as carrier for pulmonary administration. AAPS Pharm Sci Technol, 2004;5(2):17–23
   Web of Science ®Google Scholar
• Sarkar NN. Mifepristone: Bioavailability, pharmacokinetics and useful-effectiveness. Eur J Obstet Gynaecol Reprod Biol, 2002;101:113–20
   PubMed Web of Science ®Google Scholar
• Semete B, Kalombo L, Katata L, Swai H. 2010. Nano-drug delivery systems: Advances in TB, HIV and malaria treatment. In: Mishra AK, Tiwari A, Mishra SB, eds. Smart biomolecular medicine. Allahabad, India: VBRI Press, pp. 15–52
   Google Scholar
• Shapiro TA, Goldberg DA. 2006. Analgesic-antipyretic and anti-inflammatory agents; pharmacotherapy of gout. In: Goodman and Gilman’s the pharmacological basis of therapeutics, 11th ed. USA: McGraw-Hill Medical Publishing Division, pp. 1021–7
   Google Scholar
• Singh J, Gupta S, Kaur H. Prediction of in vitro drug release mechanisms from extended release matrix tablet using SSR/SR2 techniques. Trends App Sci Res, 2011;6(4):400–9
   Google Scholar
• Singh RM, Singh D, Swarnlata S. Development and in vitro evaluation of polar lipid based lipospheres for oral delivery of peptide drugs. Int J Drug Deliv, 2009;1:15–26
   Google Scholar
• Snow RW, Querra CA, Noor AM, Myint HY, Hay SI. The global distribution of clinical episodes of Plasmodium falciparium malaria. Nature, 2005;434:214–17
   PubMed Web of Science ®Google Scholar
• Souza VD, De Man JM. Short spacing and polymorphic forms of natural and commercial solid fats: A review. J Am Oil Chem Soc, 1990;67:835–43
   Web of Science ®Google Scholar
• Thanh NV, Cowman AF, Hipgrave D, Kim TB, Phuc BQ, Cong LD, Biggs BA. Assessment of susceptibility of Plasmodium falciparum to Chloroquine, Quinine, Mefloquine, Sulphadoxine-Pyrimethamine and Artemisinin in Southern Vietnam. Trans. Royal Soc Trop Med Hyg, 2009;95:513–17
   Google Scholar
• Umeyor EC, Kenechukwu FC, Ogbonna JD, Chime SA, Attama AA. Preparation of novel solid lipid microparticles loaded with gentamicin and its evaluation in vitro and in vivo. J Microencapsul, 2012;29(3):296–307
   PubMed Web of Science ®Google Scholar
• You J, Cui F, Zi Q, Han X, Yu Y, Yang M. A novel formulation design about water insoluble oily drug: Preparation of Zedoaryl tumeric oil microspheres with self emulsifying ability and evaluation in rabbits. Int J Pharm, 2005;288:315–23
   PubMed Web of Science ®Google Scholar