Abstract
Background: The high molecular weight and increasing lipophilicity of drug
face many problems starting from the drug development to formulation and conduction of
pharmacological, toxicological and pharmacokinetic studies to its biological application.
To overcome this problem, nano-sized formulations are in trend recently. The use of Solid
lipid nanoparticles (SLNs) offers new insight into the formulation of the poor soluble and
low bioavailable drug.
Objective: The study aimed to investigate the literature concerning the development of
SLNs for oral drug delivery of poorly soluble drugs, with a view survey the various methods
of manufacturing and evaluation of formulation of SLNs and future prospects of SLNs
and application of SLNs in oral delivery systems.
Conclusion: Oral drug delivery is looking ahead progressively into newer directions due
to the realization of various poor performance limiting factors such as reduced drug solubility
or absorption, rapid metabolism, high actuation in plasma level of drug and variability
caused due to food effect. These play a vital role in disappointing in vivo results, which
leads in the failure of the conventional delivery system. Since the last decade, oral drug
delivery has taken a new dimension with the increasing application of SLNs as a carrier
for the delivery of poorly water-soluble or lipophilic drugs. The site-specific and sustained
release effect of the drug is better achieved by using SLNs. This review highlights the various
pros and cons, manufacturing techniques, characterization, and future prospects of
SLNs in oral drug delivery systems.
Keywords:
Oral drug delivery, novel drug delivery system (NDDS), solid lipid nanoparticles (SLNs),
bioavailability, nano-sized formulations, drug solubility.
Graphical Abstract
[6]
Couvreur P, Dubernet C, Puisieux F. Controlled drug delivery with nanoparticles: current possibilities and future trends. Eur J Pharm Biopharm 1995; 41: 2-13.
[19]
Verma S, Makkar D. Solid lipid nanoparticles: a comprehensive review. J Chem Pharm Res 2016; 8(8): 102-14.
[20]
Bagul US, Pisal VV, Solanki NV, et al. A current status of solid lipid nanoparticles: A Review. Mod Appl Bioequiv 2018; 3(4): 1-10.
[21]
Pandey P, Gupta PC, Yadav S. Solid lipid nanoparticle: a potential approach in drug delivery system. Ejpmr 2018; 5(9): 225-36.
[22]
Nikam S, Mayura C, Sharma PH. Solid lipid nanoparticles: a lipid-based drug delivery. IPP 2014; 2(3): 365-76.
[23]
Shazly GA. Ciprofloxacin controlled-solid lipid nanoparticles: characterization in vitro release and antibacterial activity assessment. BioMed Res Int 2017; 4: 1-9.
[26]
Ekambaram P, Sathali A, Priyanka K. Solid lipid nanoparticles: a review. Sci Rev Chem Commun 2012; 2(1): 80-102.
[28]
Yadav V, Mahor A, Prajapati S, et al. Solid lipid nanoparticles (SLN): formulation by high-pressure homogenization. World J Pharm Pharm Sci 2014; 3(11): 1200-13.
[32]
Rupenagunta A, Somasundaram I, Ravichandiran V, et al. Solid lipid Nano particles-A versatile carrier system. J Pharm Res 2011; 4(7): 2069-75.
[33]
Rabinarayan P, Padilama S. Production of solid lipid nanoparticles-drug loading and release mechanism. J Chem Pharm Res 2010; 2(1): 211-27.
[34]
Nair R, Kumar KSA, Priya KV, et al. Recent Advances in solid lipid nanoparticle-based drug delivery systems. J Biomed Sci Res 2011; 3(2): 368-84.
[36]
Montes A, Gordillo MD, Pereyra C, et al. Particles formation using supercritical fluids. Mass transfer - advanced aspects 2011; 461-80.
[39]
Teja VRC, Chowdary VH, Raju VP, et al. A glimpse on solid lipid nanoparticles as drug delivery systems. J Glob Trends Pharm Sci 2014; 5(2): 1649-57.
[40]
Yadav N, Khatak S, Sara UVS. Solid lipid nanoparticles- a review. Int J App Pharm 2013; 5(2): 8-18.
[52]
Doktorovov_a S, Santos DL, Costa I, et al. Cationic solid lipid nanoparticles interfere with the activity of antioxidant enzymes in hepatocellular carcinoma cells. Int J Pharm 2014; 47: 118-27.
[56]
Radtke M, Souto EB, Muller RH. NLC-the novel generation of solid lipid carriers Pharm Tech Europe 2000; 517: 45-50.
[63]
Muller RH, Runge SA. Solid lipid nanoparticles for controlled drug delivery Submicron emulsion in drug targeting and delivery. The Netherlands: Harwood Academic Publishers 1998; pp. 219-34.