Successfully reported this slideshow.
We use your LinkedIn profile and activity data to personalize ads and to show you more relevant ads. You can change your ad preferences anytime.

are nanostructured lipid carrier are better then solid lipid nanoparticles

2,632 views

Published on

Comparative study between solid lipid nanoparticles and nanostrucuted lipid carrier

Published in: Education, Technology, Business
  • Be the first to comment

are nanostructured lipid carrier are better then solid lipid nanoparticles

  1. 1. Are nanostructured lipid carriers (NLCs) better than solid lipid nanoparticles(SLNs): Development, characterizations and comparative evaluations of clotrimazole- loaded SLNs and NLCs? Presented by Devendra singh
  2. 2. Contents Introduction. Material and methods. Characterization. Result and discussion. Conclusion.
  3. 3. Introduction  From the recent past, biocompatible lipids have been attracting the attention of the formulation scientists as carriers for the delivery of poorly soluble drugs (Pouton, 2006).  Among biocompatible lipids, lipid nanoparticle formulations with solid matrix have gained huge popularity.  Generally, there are two types of lipid nanoparticles with solid matrix, solid lipid nanoparticles (SLNs) and nanostructured lipid carriers (NLCs) (Das and Chaudhury, 2011).  Theses nanoparticles can be widely applied to deliver drugs/actives through oral, parenteral and topical routes (Almeida and Souto, 2007; Das and Souto, 2007.  However, the current focus of the SLNs and NLCs research is more inclined towards topical (especially dermal) application both in pharmaceutical and cosmetic purposes (Pardeike et al., 2009).
  4. 4. SLNs are beneficial in many aspects such as:  possess negligible toxicity.  lipophilic compounds can be easily encapsulated.  bioavailability of highly lipophilic molecules can be increased via lymphatic uptake.  degradation of chemical/moisture/light/oxidation sensitive molecules can be prevented by their incorporation in the nanoparticle matrix.  sustained drug release from the nanoparticle matrix is possible due to solid nature of the matrix leading to prolonged drug release.  penetration through skin or mucus barrier is possible due to nano size.
  5. 5. drawbacks of SLNs  polymorphic transitions of the lipid may occur with time due to the crystalline structure of solid lipid (Müller et al., 2002).  Lipid crystallizes in high-energetic lipid modifications, α and β immediately after preparation of SLNs.  In general, drug molecules stay in between the fatty acid chains or as amorphous clusters in crystal imperfections within SLN matrix. But, when lipid transform to low- energetic form, it form a perfect crystalline lattice that allows very small space for the drug molecules. Therefore, expulsion of encapsulated drug molecules may be observed during storage which leads to limited drug-loading capacity of SLNs.
  6. 6. NLCs as alternate drug carrier systems over SLNs  In the process of further improvement and reduction of these drawbacks of SLNs, NLCs have been evolved as alternative drug carrier systems.  NLC matrix is composed of mixture of spatially different lipid molecules, normally mixture of solid and liquid lipid, which makes more imperfection in the matrix to accommodate more drug molecules than SLN.  It is expected that the drug-loading capacity will be enhanced, drug expulsion during storage will be minimized due to the imperfect crystal lattice and drug release profile can be easily modulated by varying the lipid matrix composition (Müller et al., 2002a; Radtke et al., 2005).
  7. 7. Formulation technique: Emulsification ultra sonication technique: Melted lipid or lipid mixture o/w Nano emulsion Immediately placed in double walled plastic box filled with ice to cool it down The liquid nano-droplet transformed into solid nanoparticles dispersions Coarse o/w emulsion drug hot aqueous surfactant solution homogenize at 14000- 15000rpm Sonication at 75 c In case of SLNs solid lipid was weighed and heated 75 c In case of NLCs solid and liquid lipid heated 75 c
  8. 8. Characterization Particle size, polydispersity index and zeta potential measurement:  For particle size and polydispersity index measurements, the diluted nanoparticle dispersion was poured into the disposable sizing cuvette which was then placed in the cuvette holder of the instrument and analyzed using the zetasizer software (DTS v 6.12, Malvern Instruments, UK).  For zeta potential measurement, disposable folded capillary cuvette was used. Air bubbles, if any, were removed from the capillary before measurement. All measurements were performed in triplicate.
  9. 9. Drug loading and encapsulation efficiency measurement: Drug loading and encapsulation efficiency were determined by measuring the amount of encapsulated drug within the nanoparticles (Das et al., 2011). Unencapsulated insoluble drug (if any) were first filtered out through 3lm nitrocellulose membrane filter. Then, methanol (9.5 mL) was added in the filtered formulation(0.5 mL) and mixed well with the help of a cyclomixer. then centrifuged for 15 min at 5000 rpm and supernatant was collected. The drug concentration in the supernatant was measured by HPLC Drug encapsulation efficiency (EE) and drug loading (L) were calculated using the following equations: EE(%)= actual amount of drug in the filtered formulation-soluble unencapsulated drug x100 amount of drug added during formulation L(%) = actual amount of encapsulated drug x100 amount of lipid used to prepare the formulation
  10. 10. Scanning electron microscopy study  Some researchers have used SEM for the morphology of SLNs (Varshosaz et al., 2010), the nanoparticles may not maintain their integrity and solid state during SEM analysis due to the increase in energy during measurment. Therefore, cryogenic field emission scanning electron microscopy was used to examine shape, size and surface morphology of the SLNs/NLCs.  few drops of the nanoparticle dispersion were placed on a copper stub and frozen in nitrogen slush at -196 C. The frozen sample was then stored in liquid nitrogen and transferred into the cryo preparation chamber attachedto a FESEM where the frozen sample was freeze-fractured, sublimed for 30 s at -95 C and sputtercoated with platinum for 120 s. Then the coated sample was placed onto the specimen stage of the FESEM at140 C and analyzed at an excitation voltage of 5 kV.
  11. 11. Differential scanning calorimetry analysis  Firstly SNLs and NLCs samples are lyophilized, filled and blank NLCs and SLNs were subjected to DSC.  samples(4–5 mg) were kept in the standard aluminum pans and sealed. Then the pans were placed under isothermal condition at 25 C for 10 min. DSC analysis was performed at 10 C/min from 25 to 290C under a inert environment. An empty sealed pan was used as reference. The thermograms of the samples were recorded
  12. 12. Drug release study The dialysis bag method was followed for the drug release study The day before the drug release experiment, dialysis tube (10 kDa molecular cut off) was treated closely following the protocol (Sigma) and soaked in the release media overnight. Phosphate buffer at pH 7.4 containing 2% Tween 80 was used as drug release media. Accurately measured 1 mL formulation was placed in the dialysis tube and both end of the tube was tightly tied to prevent any leakage. The tube containing formulation was then kept in an amber colored glass bottle containing 10 mL release media. The bottle was kept on a horizontal rotary shaker rotating at 100 rpm. Samples (5 mL release media) were withdrawn from the bottle at the predetermined time intervals and replaced by 5 mL fresh release media. The samples were then analyzed by HPLC to determine the amount of drug released from the formulation at different time points.
  13. 13. Results and Discussion
  14. 14. Particle size  Particle size measurement was required to confirm the production of the particles in nano- range.  particle size was significantly influenced by most of the formulation and process variables.  Among the different lipid tested, SLNs prepared using Compritol 888ATO were smallest and SLNs prepared using Dynasan 118 were biggest.  However, no relationship between chemical structure of the lipids and particle size was observed. This might be because of the complex structure of these lipids.
  15. 15. Effect of surfactant on particle size  Among the 4 non-ionic surfactant tested, SLNs prepared using Chremophore EL demonstrated lowest size, whereas SLNs prepared using PluronicF68 demonstrated largest size (fig.b)  Hydrophilic-lipophilic balance (HLB) value of 12–16 is considered to be ideal for the production of stable o/w emulsion.  In contrast, HLB value of Pluronic F68 is very high (>24). This might be the main reason of bigger particle size when PluronicF68 was used.
  16. 16. Effect of sonication time on particle size. Particle size dramatically decreased with increasing sonication time However, the size reduction was not huge above 10 min sonication time. (Fig. 1C)
  17. 17. Particle size dramatically decreased with increasing surfactant concentration (Fig. 1D).
  18. 18. Polydispersity index  Polydispersity index (PI) indicates the width of the particle size distribution, which ranges from 0 to 1.  Theoretically, monodisperse populations indicates PI = 0. However, PI < 0.2 is considered as narrow size distribution.  Among the lipids, Compritol 888ATO produced SLNs with lowest PI and Geleol™ produced SLNs with highest PI (Fig. 1A).  Among the surfactants Chremophore EL produced SLNs with lowest PI and Pluronic F68 produced SLNs with highest PI (Fig. 1B).  PI decreased with increasing sonication time (up to 15 min) and surfactant concentration. PI was very high at 1–5 min sonication time and 0.5–1% surfactant concentration.
  19. 19. Zeta potential  ZP refers to the surface charge of the particles. ZP ( ) indicates the degree of repulsion between close and similarly charged particles in the dispersion.  This repulsion force prevents aggregation of the particles. Therefore, ZP is a useful parameter to predict the physical stability of the SLN/NLC dispersions (Das and Chaudhury, 2011; Freitas and Müller, 1998).  The results indicate that ZP values were less than -20 mV for all prepared SLNs and NLCs, except SLNs prepared at 1% lipid concentration.  ZP of the SLNs prepared with different lipids decreased as follows: Precirol ATO5 > Compritol 888ATO > Suppocire NC > Geleol™ > Dynasan 114 > Imwitor 900 K > Dynasan118 (Fig. 1A)  There was no specific correlation between ZP and solid to liquid lipid ratio in NLCs (Fig. 2A).
  20. 20. Drug encapsulation efficiency  Drug encapsulation efficiency (EE) was highest and lowest when SLNs were prepared with Compritol 888ATO (>87%) and Dynasan 118 (<76%) as lipid, respectively (Fig. 1A).  SLNs prepared with Chromophore EL as surfactant showed highest EE (>87%) (Fig. 1B). However, EE was > 79% when SLNs prepared with other surfactants too.  The results showed that EE of SLNs was not dependant on sonication time (Fig. 1C).  EE of SLNs significantly increased with increasing surfactant concentration.  However, insignificant increase in EE was noticed above 2% surfactant concentration. (Fig. 1D).
  21. 21. Scanning electron microscopy  The images indicate that both SLNs and NLCs were spherical with size between 50 and 150 nm. Although it was not common, some particle agglomerates were observed (Fig. 3C).  The particle aggregations might be due to sticky nature of the lipid.  Surface morphology of both SLNs and NLCs were smooth and there is no visible difference between them (Fig. 3B–D).  The crystalline structures of clotrimazole were absent in the SEM images of SLNs and NLCs, which suggests absence of unencapsulated undissolved drug crystals in the dispersions.
  22. 22. Fig. 3. SEM images of clotrimazole (A), solid lipid nanoparticles (B and C) and nanostructured lipid carriers (D)
  23. 23. Drug release  Cumulative drug release from the nanoparticle dispersions were plotted against time (Fig.6).  SLNs and NLCs prepared at 4% drug to lipid ratio showed sustained and prolonged drug release. However, drug release rate of NLCs 4% was significantly faster than SLN-4% . (Fig. 6A)  Both SLNs and NLCs prepared at 8% drug to lipid ratio (i.e., SLN-8% and NLC- 8%) showed significantly slower drug release rate than their counterparts with 4% drug to lipid ratio.  There was no significant difference in drug release profile or rate between SLN-8% and NLC-8% .  There was also no significant difference in drug release profile of NLCs after 3 months storage in compare to fresh NLCs, while significant change drug release rate was observed in case of SLNs.
  24. 24. Drug release plots. Comparison of drug release from SLNs and NLCs at 4% (SLN-4% and NLC-4%) and 8% (SLN-8% and NLC-8%) drug to lipid ratio (A). Effect of release media volume (10 mL versus 20 mL) on drug release from SLN-8% (B). Effect of dilution of SLNs-4% on drug release (C). Comparison of drug release from fresh and 3 months old SLN-4% and NLC-4% stored at 2–8C (D). Data represent mean SD (n= 3).
  25. 25. Drug release contd..  lower drug release at 8% drug to lipid ratio than 4% drug to lipid ratio might be due to absence of proper sink condition during drug release study as drug amount was doubled but volume of release media was same (10 mL).  Therefore, another drug release experiment was performed on SLNs prepared with 8% drug to lipid ratio using 20 mL release media. The result indicates slightly faster drug release when 20 mL release media was used than 10 mL release media. (Fig. 6B)  In another experiment, effect of dilution of formulation on drug release was investigated. The experiment was performed as formulation is diluted after oral ingestion (in gastric fluid) or intravenous injection (in blood), whereas almost no dilution occur during topical application on skin. In this experiment, SLN dispersion was diuted 5 times with ultrapure water and then release study was performed in 10 mL release media (Fig. 6C).
  26. 26. Conclusion  The study suggests the importance of controlling the critical formulation and process parameters during formulation as they greatly influenced the final product, such as particle size, polydispersity index, zeta potential, drug encapsulation efficiency.  Chemical characterizations (DSC) demonstrated slight difference in crystal structure between SLNs and NLCs, although crystalline peak(s) of clotrimazole disappeared in both SLNs and NLCs.  Sustained drug release was observed from SLNs and NLCs. NLCs exhibit the same release pattern after 3 month as fresh, while significant change was observed in case of SLNs  In the comparative study, NLCs exhibited faster drug release than SLNs at the low drug-loading.  Both tested SLNs and NLCs were stable at 2–8 C even at high drug-loading and also stable at 25 c at low drug loading. therefore, NLCs have an edge over SLNs.  Although both SLN and NLCs can be used as effective carrier of lipophilic drugs depending on desired drug release profile, NLCs might be better option than SLNs. Nevertheless different stabilizing route need to be evaluated in near future.
  27. 27. Reference  Das S, Ng Wai K, Tan R. “Are nanostructured lipid carriers (NLCs) better than solid lipid nanoparticles(SLNs): Development, characterizations and comparative evaluations of clotrimazole-loaded SLNs and NLCs?” Euro. Jur. Of ph sci. june 1, 2012.
  28. 28. Thank you

×