Abstract
The use of current treatments for poverty-related diseases (PRDs) is compromised due to factors such as toxicity and poor solubility leading to lowered bioavailability and thus reduced efficacy. In addition, there is lack of activity from the pharmaceutical industry due to the difficulty in refinancing the high development costs. Hence, new approaches have to be explored for the treatment of PRDs. Nanotechnology-based drug delivery systems (nanomedicine) offer a possible solution by presenting the ability to alter the pharmacokinetics of the conventional drugs to enhance bioavailability, increase the half-life of the drugs and reduce the toxicity. The advantages that nanomedicine-based drug delivery systems present in the treatment of PRDs and the progress of its application in Africa are summarised in this chapter. Nanodrug delivery systems seem to be a promising and viable strategy for improving treatment of PRDs and should urgently be considered in drug development programmes in Africa.
This is a preview of subscription content, log in via an institution.
Buying options
Tax calculation will be finalised at checkout
Purchases are for personal use only
Learn about institutional subscriptionsAbbreviations
- ACTs:
-
Artemisinin-based combination therapies
- ADME:
-
Absorption, distribution, metabolism and excretion
- ARV:
-
Antiretroviral
- AUC:
-
Area under the curve
- C max :
-
Maximum plasma concentration
- CYP:
-
Cytochrome P450
- ESE:
-
Emulsion-solvent-evaporation
- ESSE:
-
Emulsion-solvent-surfactant-evaporation
- ETB:
-
Ethambutol
- HIV:
-
Human immunodeficiency virus
- INH:
-
Isoniazid
- IV:
-
Intravenous
- MIC:
-
Minimum inhibitory concentration
- NTDs:
-
Neglected tropical diseases
- PBCA:
-
Poly(butyl-2-cyanoacrylate)
- PCL:
-
Polycaprolactone
- PEG:
-
Polyethylene glycol
- PK:
-
Pharmacokinetics
- PLGA:
-
Poly(D,L-lactic-co-glycolic acid)
- PRDs:
-
Poverty-related diseases
- PZA:
-
Pyrazinamide
- RES:
-
Reticuloendothelial system
- RECG:
-
Reverse-emulsion-cationic-gelification
- RESCG:
-
Reverse-emulsion-surfactant-cationic-gelification
- RIF:
-
Rifampicin
- R&D:
-
Research and development
- TB:
-
Tuberculosis
References
Bawa R, Bawa SR, Maebius SB et al (2005) Protecting new ideas and inventions in nanomedicine with patents. Nanomedicine 1:150–158
Mishra B, Patel BB, Tiwari S (2010) Colloidal nanocarriers: a review on formulation technology, types and applications toward targeted drug delivery. Nanomedicine 6:9–24
Malam Y, Loizidou M, Seifalian AM (2009) Liposomes and nanoparticles: nanosized vehicles for drug delivery in cancer. Trends Pharmacol Sci 30:592–599
WHO (2010) Global tuberculosis control: WHO report 2010. World Health Organisation, Geneva
WHO (2010) World malaria report 2010. World Health Organisation, Geneva
UNAIDS (2010) UNAIDS report on the global AIDS epidemic
Davidson RN (2005) Leishmaniasis. Medicine 33:43–46
Anwabani GM (2002) Drug development: a perspective from Africa. Paediatr Perinat Drug Ther 5:4–11
Choonara YE, Pillay V, Ndesendo VMK et al (2011) Polymeric emulsion and crosslink-mediated synthesis of super-stable nanoparticles as sustained-release anti-tuberculosis drug carriers. Colloids Surf B Biointerfaces 87:243–254
Semete B, Booysen L, Lemmer Y et al (2010) In vivo evaluation of the biodistribution and safety of PLGA nanoparticles as drug delivery systems. Nanomedicine 6:662–671
Semete B, Booysen LI, Kalombo L et al (2010) In vivo uptake and acute immune response to orally administered chitosan and PEG coated PLGA nanoparticles. Toxicol Appl Pharmacol 249:158–165
Swai H, Semete B, Kalombo L et al (2008) Potential of treating tuberculosis with a polymeric nano-drug delivery system. J Control Release 132:e48
Ma Z, Lienhardt C, McIlleron H et al (2010) Global tuberculosis drug development pipeline: the need and the reality. Lancet 375:2100–2109
http://www.novartisoncology.com/research-innovation/pipeline.jsp. Accessed 22 July 2011
Jang GR, Harris RZ, Lau DT (2001) Pharmacokinetics and its role in small molecule drug discovery research. Med Res Rev 21:382–396
http://hivinsite.ucsf.edu/InSite?page=ar-01-03. Accessed 23 June 2011
Nzila A, Chilengi R (2010) Modulators of the efficacy and toxicity of drugs in malaria treatment. Trends Pharmacol Sci 31:277–283
Grimberg BT, Mehlotra RK (2011) Expanding the antimalarial drug arsenal-now, but how? Pharmaceuticals (Basel) 4:681–712
Chatelain E, Ioset JR (2011) Drug discovery and development for neglected diseases: the DNDi model. Drug Des Devel Ther 5:175–181
Kola I, Landis J (2004) Can the pharmaceutical industry reduce attrition rates? Nat Rev Drug Discov 3:711–715
Riviere JE (2009) Pharmacokinetics of nanomaterials: an overview of carbon nanotubes, fullerenes and quantum dots. Wiley Interdiscip Rev Nanomed Nanobiotechnol 1:26–34
Couvreur P, Vauthier C (2006) Nanotechnology: intelligent design to treat complex disease. Pharm Res 23:1417–1450
Gelperina S, Kisich K, Iseman MD et al (2005) The potential advantages of nanoparticle drug delivery systems in chemotherapy of tuberculosis. Am J Respir Crit Care Med 172:1487–1490
Li SD, Huang L (2008) Pharmacokinetics and biodistribution of nanoparticles. Mol Pharm 5:496–504
Pandey R, Ahmad Z, Sharma S et al (2005) Nano-encapsulation of azole antifungals: potential applications to improve oral drug delivery. Int J Pharm 301:268–276
Medina C, Santos-Martinez MJ, Radomski A et al (2007) Nanoparticles: pharmacological and toxicological significance. Br J Pharmacol 150:552–558
Kingsley JD, Dou H, Morehead J et al (2006) Nanotechnology: a focus on nanoparticles as a drug delivery system. J Neuroimmune Pharmacol 1:340–350
McNeil SE (2005) Nanotechnology for the biologist. J Leukoc Biol 78:585–594
Desai MP, Labhasetwar V, Walter E et al (1997) The mechanism of uptake of biodegradable microparticles in Caco-2 cells is size dependent. Pharm Res 14:1568–1573
Koziara JM, Lockman PR, Allen DD et al (2003) In situ blood-brain barrier transport of nanoparticles. Pharm Res 20:1772–1778
Park JH, Saravanakumar G, Kim K et al (2010) Targeted delivery of low molecular drugs using chitosan and its derivatives. Adv Drug Deliv Rev 62:28–41
Freiberg S, Zhu XX (2004) Polymer microspheres for controlled drug release. Int J Pharm 282:1–18
Mohanraj VJ, Chen Y (2006) Nanoparticles – a review. Trop J Pharm Res 5:561–573
Kondo N, Iwao T, Kikuchi M et al (1993) Pharmacokinetics of a micronized, poorly water-soluble drug, HO-221, in experimental animals. Biol Pharm Bull 16:796–800
Mittal G, Sahana DK, Bhardwaj V et al (2007) Estradiol loaded PLGA nanoparticles for oral administration: effect of polymer molecular weight and copolymer composition on release behavior in vitro and in vivo. J Control Release 119:77–85
Kumari A, Yadav SK, Yadav SC (2010) Biodegradable polymeric nanoparticles based drug delivery systems. Colloids Surf B Biointerfaces 75:1–18
Bae Y, Kataoka K (2009) Intelligent polymeric micelles from functional poly(ethylene glycol)-poly(amino acid) block copolymers. Adv Drug Deliv Rev 61:768–784
Gaucher G, Dufresne MH, Sant VP et al (2005) Block copolymer micelles: preparation, characterization and application in drug delivery. J Control Release 109:169–188
Jones M, Leroux J (1999) Polymeric micelles – a new generation of colloidal drug carriers. Eur J Pharm Biopharm 48:101–111
Svenson S, Tomalia DA (2005) Dendrimers in biomedical applications–reflections on the field. Adv Drug Deliv Rev 57:2106–2129
Muller RH, Mader K, Gohla S (2000) Solid lipid nanoparticles (SLN) for controlled drug delivery – a review of the state of the art. Eur J Pharm Biopharm 50:161–177
Couvreur P, Barratt G, Fattal E et al (2002) Nanocapsule technology: a review. Crit Rev Ther Drug Carrier Syst 19:99–134
Sosnik A, Carcaboso AM, Glisoni RJ et al (2010) New old challenges in tuberculosis: potentially effective nanotechnologies in drug delivery. Adv Drug Deliv Rev 62:547–559
Semete B, Kalombo L, Katata L et al. (2011) Potential of improving the treatment of tuberculosis through nanomedicine. Mol Cryst Liq Cryst 556:317–330
Trewyn BG, Nieweg JA, Zhao Y et al (2008) Biocompatible mesoporous silica nanoparticles with different morphologies for animal cell membrane penetration. Chem Eng J 137:23–29
Benadie Y, Deysel M, Siko DG et al (2008) Cholesteroid nature of free mycolic acids from M. tuberculosis. Chem Phys Lipids 152:95–103
Lemmer Y, Semete B, Booysen L et al (2008) Targeted nanodrug delivery systems for the treatment of tuberculosis. Drug Discov Today 15:1098
Murray HW, Berman JD, Davies CR et al (2005) Advances in leishmaniasis. Lancet 366:1561–1577
Abdulla M-H, Lim K-C, Sajid M et al (2007) Schistosomiasis mansoni: Novel chemotherapy using a cysteine protease inhibitor. PLoS Med 4:130–138
Islam RU, Hean J, van Otterlo WAL et al (2009) Efficient nucleic acid transduction with lipoplexes containing novel piperazine- and polyamine-conjugated cholesterol derivatives. Bioorg Med Chem Lett 19:100–103
Arbuthnot P (2009) Applying nanotechnology to gene therapy for treatment of serious viral infections. Nano News, South Africa. http://www.sani.org.za/pdf/NanoNovember09.pdf. Accessed 24 Oct 2011
Steyn JD, Wiesner L, du Plessis LH et al (2011) Absorption of the novel artemisinin derivatives artemisone and artemiside: potential application of Pheroid technology. Int J Pharm 414:260–266
Lowell JE, Earl CD (2009) Leveraging biotech’s drug discovery expertise for neglected diseases. Nat Biotechnol 27:323–329
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2012 Springer Berlin Heidelberg
About this chapter
Cite this chapter
Hayeshi, R. et al. (2012). Nanomedicine in the Development of Drugs for Poverty-Related Diseases. In: Chibale, K., Davies-Coleman, M., Masimirembwa, C. (eds) Drug Discovery in Africa. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-28175-4_17
Download citation
DOI: https://doi.org/10.1007/978-3-642-28175-4_17
Published:
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-28174-7
Online ISBN: 978-3-642-28175-4
eBook Packages: Chemistry and Materials ScienceChemistry and Material Science (R0)