journal article·2015-11

Chemical approach to solvent removal during nanoencapsulation: its application to preparation of PLGA nanoparticles with non-halogenated solvent

Youngme Lee, Eric Sah, Hongkee Sah

Journal of Nanoparticle Research· Volume 17· Issue 11
Publisher page

Abstract

The objective of this study was to develop a new oil-in-water emulsion-based nanoencapsulation method for the preparation of PLGA nanoparticles using a non-halogenated solvent. PLGA (60–150 mg) was dissolved in 3 ml of methyl propionate, which was vortexed with 4 ml of a 0.5–4 % polyvinyl alcohol solution. This premix was sonicated for 2 min, added into 30 ml of the aqueous polyvinyl alcohol solution, and reacted with 3 ml of 10 N NaOH. Solvent removal was achieved by the alkaline hydrolysis of methyl propionate dissolved in an aqueous phase into water-soluble methanol and sodium propionate. It was a simple but effective technique to quickly harden nanoemulsion droplets into nanoparticles. The appearing PLGA nanoparticles were recovered by ultracentrifugation and/or dialysis, lyophilized with trehalose, and redispersed by water. This nanoencapsulation technique permitted a control of their mean diameters over 151.7 ± 3.8 to 440.2 ± 22.2 nm at mild processing conditions. When the aqueous polyvinyl alcohol concentration was set at ≥1 %, nanoparticles showed uniform distributions with polydispersity indices below 0.1. There were no significant changes in their mean diameters and size distribution patterns before and after lyophilization. When mestranol was encapsulated into nanoparticles, the drug was completely nanoencapsulated: depending on experimental conditions, their encapsulation efficiencies were determined to be 99.4 ± 7.2 to 105.8 ± 6.3 %. This simple, facile nanoencapsulation technique might have versatile applications for the preparation of polymeric nanoparticulate dosage forms. Schematic illustration of an innovative chemical approach to solvent removal during nanoencapsulation. Methyl propionate present in the aqueous continuous phase reacts with sodium hydroxide, thereby producing methanol and sodium propionate. Its alkaline hydrolysis allows the continuous extraction of the solvent out of nanoemulsion droplets, eventually solidifying them into nanoparticles. It is a simple but effective nanoencapsulation technique that has advantages over typical solvent evaporation and/or extraction methods.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Nanoparticle-Based Drug Delivery · Advanced Drug Delivery Systems · Pickering emulsions and particle stabilization

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (54)

Show source-provided references
1. Alonso-Sande M, des Rieux A, Fievez V, Sarmento B, Delgado A, Evora C, Remuñán-López C, Préat V, Alonso MJ (2013) Development of PLGA-mannosamine nanoparticles as oral protein carriers. Biomacromolecules 14:4046–405210.1021/bm401141u ↗
2. Bala I, Hariharan S, Kumar MN (2004) PLGA nanoparticles in drug delivery: the state of the art. Crit Rev Ther Drug Carrier Syst 21:387–42210.1615/CritRevTherDrugCarrierSyst.v21.i5.20 ↗
3. Beck-Broichsitter M, Rytting E, Lebhardt T, Wang X, Kissel T (2010) Preparation of nanoparticles by solvent displacement for drug delivery: a shift in the “ouzo region” upon drug loading. Eur J Pharm Sci 41:244–25310.1016/j.ejps.2010.06.007 ↗
4. Birnbaum DT, Kosmala JD, Brannon-Peppas L (2000) Optimization of preparation techniques for poly(lactic acid-co-glycolic acid). J Nanopart Res 2:173–18110.1023/A:1010038908767 ↗
5. Boonyasirisri P, Nimmannit U, Rojsitthisak P, Bhunchu S, Rojsitthisak P (2015) Optimization of curcuminoid-loaded PLGA nanoparticles using Box-Behnken statistical design. J Nano Res 33:60–7110.4028/www.scientific.net/JNanoR.33.60 ↗
6. Budhian A, Siegel SJ, Winey KI (2005) Production of haloperidol-loaded PLGA nanoparticles for extended controlled drug release of haloperidol. J Microencapsul 22:773–78510.1080/02652040500273753 ↗
7. Chowdhury S, Guha R, Trivedi R, Kompella UB, Konar A, Hazra S (2013) Pirfenidone nanoparticles improve corneal wound healing and prevent scarring following alkali burn. PLoS ONE 8:e7052810.1371/journal.pone.0070528 ↗
8. Cohen H, Levy RJ, Gao J, Fishbein I, Kousaev V, Sosnowski S, Slomkowski S, Golomb G (2000) Sustained delivery and expression of DNA encapsulated in polymeric nanoparticles. Gene Ther 7:1896–190510.1038/sj.gt.3301318 ↗
9. Cohen-Sela E, Chorny M, Koroukhov N, Danenberg HD, Golomb G (2009) A new double emulsion solvent diffusion technique for encapsulating hydrophilic molecules in PLGA nanoparticles. J Control Release 133:90–9510.1016/j.jconrel.2008.09.073 ↗
10. Cun D, Foged C, Yang M, Frøkjaer S, Nielsen HM (2010) Preparation and characterization of poly(DL-lactide-co-glycolide) nanoparticles for siRNA delivery. Int J Pharm 390:70–7510.1016/j.ijpharm.2009.10.023 ↗
11. Dalwadi G, Benson HAE, Chen Y (2005) Comparison of diafiltration and tangential flow filtration for purification of nanoparticle suspensions. Pharm Res 22:2152–216210.1007/s11095-005-7781-z ↗
12. Danhier F, Ansorena E, Silva JM, Coco R, Breton Le, Préat V (2012) PLGA-based nanoparticles: an overview of biomedical applications. J Control Release 161:505–52210.1016/j.jconrel.2012.01.043 ↗
13. Ganachaud F, Katz JL (2005) Nanoparticles and nanocapsules created using the ouzo effect: spontaneous emulsification as an alternative to ultrasonic and high-shear devices. ChemPhysChem 6:209–21610.1002/cphc.200400527 ↗
14. Ganea GM, Fakayode SO, Losso JN, van Nostrum CF, Sabliov CM, Warner IM (2010) Delivery of phytochemical thymoquinone using molecular micelle modified poly(d, l-lactide-co-glycolide) (PLGA) nanoparticles. Nanotechnology 21:285104. doi: 10.1088/0957-4484/21/28/28510410.1088/0957-4484/21/28/285104 ↗
15. Godsey ME, Suryaprakash S, Leong KW (2013) Materials innovation for co-delivery of diverse therapeutic cargos. RSC Adv 3:24794–2481110.1039/c3ra43094d ↗
16. Hoang TKN, Deriemaeker L, La VB, Fins R (2004) Monitoring the simultaneous Ostwald ripening and solubilization of emulsions. Langmuir 20:8966–896910.1021/la049184b ↗
17. Im HY, Kim J, Sah H (2010) Another paradigm in solvent extraction-based microencapsulation technologies. Biomacromolecules 11:776–78610.1021/bm9013952 ↗
18. Jung T, Breitenbach A, Kissel T (2000) Sulfobutylated poly(vinyl alcohol)-graft-poly(lactide-co-glycolide) facilitates the preparation of small negatively charged biodegradable nanospheres. J Control Release 67:157–16910.1016/S0168-3659(00)00201-7 ↗
19. Kalluru R, Fenaroli F, Westmoreland D, Ulanova L, Maleki A, Roos N, Paulsen Madsen M, Koster G, Egge-Jacobsen W, Wilson S, Roberg-Larsen H, Khuller GK, Singh A, Nyström B, Griffiths G (2013) Poly(lactide-co-glycolide)-rifampicin nanoparticles efficiently clear Mycobacterium bovis BCG infection in macrophages and remain membrane-bound in phago-lysosomes. J Cell Sci 126:3043–305410.1242/jcs.121814 ↗
20. Kang J, Sah E, Sah H (2014) Applicability of non-halogenated methyl propionate to microencapsulation. J Microencapsul 31:323–33210.3109/02652048.2013.843729 ↗
21. Kapoor DN, Bhatia A, Kaur R, Sharma R, Kaur G, Dhawan S (2015) PLGA: a unique polymer for drug delivery. Ther Deliv 6:41–5810.4155/tde.14.91 ↗
22. Khalil NM, do Nascimento TCF, Casa DM, Dalmolin LF, de Mattos AC, Hoss I, Romano MA, Mainardes RM (2013) Pharmacokinetics of curcumin-loaded PLGA and PLGA–PEG blend nanoparticles after oral administration in rats. Colloid Surface B 101:353–36010.1016/j.colsurfb.2012.06.024 ↗
23. Kim TH, Jeng YI, Jin SG, Pei J, Jung TY, Moon KS, Kim IY, Kang SS, Jung S (2011) Preparation of polylactide-co-glycolide nanoparticles incorporating celecoxib and their antitumor activity against brain tumor cells. Int J Nanomedicine 6:2621–263110.2147/IJN.S19497 ↗
24. Kumar V, Prud’homme RK (2009) Nanoparticle stability: processing pathways for solvent removal. Chem Eng Sci 64:1358–136110.1016/j.ces.2008.11.017 ↗
25. Lamprecht A, Ubrich N, Yamamoto H, Schafer U, Takeuchi H, Lehr CM, Maincent P, Kawashima Y (2001) Design of rolipram-loaded nanoparticles: comparison of two preparation methods. J Control Release 71:297–30610.1016/S0168-3659(01)00230-9 ↗
26. Lepeltier E, Bourgaux C, Couvreur P (2014) Nanoprecipitation and the “Ouzo effect”: application to drug delivery devices. Adv Drug Deliv Rev 71:86–9710.1016/j.addr.2013.12.009 ↗
27. Limayen I, Charcosset C, Fessi H (2004) Purification of nanoparticle suspensions by a concentration/diafiltration process. Sep Purif Technol 38:1–910.1016/j.seppur.2003.10.002 ↗
28. Mahajan NM, Sakarkar DM, Manmode AS (2011) Preparation and characterization of meselamine loaded PLGA nanoparticles. Int J Pharm Pharm Sci 3:208–214
29. Mainardes RM, Evangelista RC (2005) PLGA nanoparticles containing praziquantel: effect of formulation variables on size distribution. Int J Pharm 290:137–14410.1016/j.ijpharm.2004.11.027 ↗
30. Mariano RN, Alberti D, Cutrin JC, Geninatti Crich S, Aime S (2014) Design of PLGA based nanoparticles for imaging guided applications. Mol Pharm 11:4100–410610.1021/mp5002747 ↗
31. Matthäus C, Schubert S, Schmitt M, Krafft C, Kietzek B, Schubert US, Popp J (2013) Resonance raman spectral imaging of intracellular uptake of β-carotene loaded poly(d, l-lactide-co-glycolide. ChemPhysChem 14:155–16110.1002/cphc.201200577 ↗
32. McCall RL, Sirianni RW (2013) PLGA nanoparticles formed by single- or double-emulsion with vitamin E-TPGS. J Vis Exp 82:e51015. doi: 10.3791/51015
33. Moinard-Checot M, Chevalier Y, Briancon S, Beney L, Fessi H (2008) Mechanism of nanocapsules formation by the emulsion–diffusion process. J Colloid Interface Sci 317:458–46810.1016/j.jcis.2007.09.081 ↗
34. Mott B, Thamake S, Vishwanatha J, Jones HP (2013) Intranasal delivery of nanoparticle-based vaccine increases protection against S. pneumonia. J Nanopart Res 15:1646. doi: 10.1007/s1105-013-1646-x10.1007/s11051-013-1646-x ↗
35. Mu L, Feng S (2003) A novel controlled release formulation for the anticancer drug paclitaxel (Taxol): PLGA nanoparticles containing vitamin E TPGS. J Control Release 86:33–4810.1016/S0168-3659(02)00320-6 ↗
36. Mura S, Hillaireau H, Nicolas J, Le Droumaguet B, Gueutin C, Zanna S, Tsapis N, Fattal E (2011) Influence of surface charge on the potential toxicity of PLGA nanoparticles towards Calu-3 cells. Int J Nanomedicine 6:2591–2605
37. Murakami H, Kobayashi M, Takeuchi H, Kawashima Y (1999) Preparation of poly(dl-lactide-co-glycolide) nanoparticles by modified spontaneous emulsification solvent diffusion method. Int J Pharm 187:143–15210.1016/S0378-5173(99)00187-8 ↗
38. Nahar M, Jain NK (2009) Preparation, characterization and evaluation of targeting potential of amphotericin B-loaded engineered PLGA nanoparticles. Pharm Res 26:2588–259810.1007/s11095-009-9973-4 ↗
39. Peça IN, Petrova KT, Cardoso MM, Barros MT (2012) Preparation and characterization of polymeric nanoparticles composed of poly(dl-lactide-co-glycolide) and poly(dl-lactide-co-glycolide)-co-poly(ethylene glycol)-10%-Triblock end-capped with a galactose moiety. React Funct Polym 72:729–73510.1016/j.reactfunctpolym.2012.06.019 ↗
40. Pillai RR, Somayaji SN, Rabinovich M, Hudson MC, Gonsalves KE (2008) Nafcillin-loaded PLGA nanoparticles for treatment of osteomyelitis. Biomed Mater 3:034114. doi: 10.1088/1748-6041/3/3/03411410.1088/1748-6041/3/3/034114 ↗
41. Rescignano N, Tarpani L, Tiribuzi R, Montesano S, Martino S, Latterini L, Kenny JM, Armentano I (2013) Protein encapsulation in biodegradable polymeric nanoparticles: morphology, fluorescence behaviour and stem cell uptake. Macromol Biosci 13:1204–121210.1002/mabi.201300140 ↗
42. Sah E, Sah H (2015) Recent trends in preparation of poly(lactide-co-glycolide) nanoparticles by mixing polymeric organic solution with antisolvent. J Nanomater, article ID 79460110.1155/2015/794601 ↗
43. Sahoo KS, Panyam J, Prabha S, Labhasetwar V (2002) Residual polyvinyl alcohol associated with poly (d, l-lactide-co-glycolide) nanoparticles affects their physical properties and cellular uptake. J Control Release 82:105–11410.1016/S0168-3659(02)00127-X ↗
44. Swaminathan SK, Roger E, Toti U, Niu L, Ohlfest JR, Panyam J (2013) CD133-targeted paclitaxel delivery inhibits local tumor recurrence in a mouse model of breast cancer. J Control Release 171:280–28710.1016/j.jconrel.2013.07.014 ↗
45. Tansik G, Yakar A, Gunduz U (2014) Tailoring magnetic PLGA nanoparticles suitable for doxorubicin delivery. J Nanopart Res 16:2171. doi: 10.1007/s11051-013-2171-710.1007/s11051-013-2171-7 ↗
46. Turk CTS, Oz UC, Serim TM, Hascicek C (2014) Formulation and optimization of nonionic surfactants emulsified nimesulide-loaded PLGA-based nanoparticles by design of experiments. AAPS PharmSciTech 15:161–17610.1208/s12249-013-0048-9 ↗
47. Vandervoort J, Ludwig A (2002) Biocompatible stabilizers in the preparation of PLGA nanoparticles: a factorial design study. Int J Pharm 238:77–9210.1016/S0378-5173(02)00058-3 ↗
48. Venier-Julienne MC, Benoît JP (1996) Preparation, purification and morphology of polymeric nanoparticles as drug carriers. Pharm Acta Helv 71:121–12810.1016/0031-6865(95)00059-3 ↗
49. Vitale SA, Katz JL (2003) Liquid droplet dispersions formed by homogeneous liquid-liquid nucleation: “The ouzo effect”. Langmuir 19:4105–411010.1021/la026842o ↗
50. Xie H, She ZG, Wang S, Sharma G, Smith JW (2012) One-step fabrication of polymeric Janus nanoparticles for drug delivery. Langmuir 28:4459–446310.1021/la2042185 ↗
51. Yin P, Wang Y, Qui Y, Hou L, Liu X, Qin J, Duan Y, Liu P, Qiu M, Li Q (2012) Bufalin-loaded mPEG-PLGA-PLL-cRGD nanoparticles: preparation, cellular uptake, tissue distribution, and anticancer activity. Int J Nanomedicine 7:3961–3969
52. Yoo HS, Lee KH, Oh JE, Park TG (2000) In vitro and in vivo anti-tumor activities of nanoparticles based on doxorubicin–PLGA conjugates. J Control Release 68:419–43110.1016/S0168-3659(00)00280-7 ↗
53. Zhang Z, Tongchusak S, Mizukami Y, Kang YJ, Ioji T, Touma M, Reinhold B, Keskin DB, Reinherz EL, Sasada T (2011) Induction of anti-tumor cytotoxic T cell responses through PLGA-nanoparticle mediated antigen delivery. Biomaterials 32:3666–367810.1016/j.biomaterials.2011.01.067 ↗
54. Zigoneanu IG, Astete CE, Sabliov CM (2008) Nanoparticles with entrapped α-tocopherol: synthesis, characterization, and controlled release. Nanotechnology 19:105606. doi: 10.1088/0957-4484/19/10/10560610.1088/0957-4484/19/10/105606 ↗