New Method to Prepare Mitomycin C Loaded PLA-Nanoparticles with High Drug Entrapment Efficiency
© to the authors 2009
Received: 10 February 2009
Accepted: 2 April 2009
Published: 21 April 2009
The classical utilized double emulsion solvent diffusion technique for encapsulating water soluble Mitomycin C (MMC) in PLA nanoparticles suffers from low encapsulation efficiency because of the drug rapid partitioning to the external aqueous phase. In this paper, MMC loaded PLA nanoparticles were prepared by a new single emulsion solvent evaporation method, in which soybean phosphatidylcholine (SPC) was employed to improve the liposolubility of MMC by formation of MMC–SPC complex. Four main influential factors based on the results of a single-factor test, namely, PLA molecular weight, ratio of PLA to SPC (wt/wt) and MMC to SPC (wt/wt), volume ratio of oil phase to water phase, were evaluated using an orthogonal design with respect to drug entrapment efficiency. The drug release study was performed in pH 7.2 PBS at 37 °C with drug analysis using UV/vis spectrometer at 365 nm. MMC–PLA particles prepared by classical method were used as comparison. The formulated MMC–SPC–PLA nanoparticles under optimized condition are found to be relatively uniform in size (594 nm) with up to 94.8% of drug entrapment efficiency compared to 6.44 μm of PLA–MMC microparticles with 34.5% of drug entrapment efficiency. The release of MMC shows biphasic with an initial burst effect, followed by a cumulated drug release over 30 days is 50.17% for PLA–MMC–SPC nanoparticles, and 74.1% for PLA–MMC particles. The IR analysis of MMC–SPC complex shows that their high liposolubility may be attributed to some weak physical interaction between MMC and SPC during the formation of the complex. It is concluded that the new method is advantageous in terms of smaller size, lower size distribution, higher encapsulation yield, and longer sustained drug release in comparison to classical method.
KeywordsMitomycin C PLA Nanoparticles Drug release
Mitomycin C (MMC) is a bifunctional alkylating agent which has been extensively used as an anti-tumor agent for a long time. Because of MMC’s enhanced activity in hypoxic environments , it has great potential for loco-regional treatment of solid tumors since a significant percentage of viable cancer cells within a solid tumor can be hypoxic . However, use of MMC is associated with a number of acute and chronic toxicities, such as irreversible myelosuppression and hemolyticuremic syndrome, which limit its clinical application. Therefore, efforts have been made to lessen the toxic effects of MMC and improve its utility using various delivery methods.
The predominant method for MMC delivery involves drug encapsulation in nano-or micro-particles using various polymers including albumin , dextran [4, 5], estradiol , N-succinyl-chitosan , hydrogels , polybutylcyanoacrylate , and poly-epsilon-caprolactone . These systems, however, have shown some defects for local administration of MMC due to fast degradation of those drug carriers in the body.
PLA is a well-known biodegradable and biocompatible polymer and has a relatively longer degradation time in vivo (from weeks to months) according to their molecular weight. It has been used in various applications such as wound dressing and drug delivery [10, 11]. Generally, the water-limited soluble MMC cannot be directly dissolved in hydrophobic organic solvents such as dichloromethane, so the drug entrapment efficiency of PLA nano/microparticles prepared by a classical double emulsion solvent evaporation method is very limited.
In order to overcome these shortcomings, we have developed a new method to prepare mitomycin C loaded PLA nanoparticles by a new emulsion solvent evaporation technique, in which soybean phosphatidylcholine (SPC) was employed to improve the liposolubility of MMC by formation of MMC–SPC complex. SPC was used because of its good biocompatibility and ready availability.
In this paper, the four main influential factors at three levels, PLA MW (molecular weight), ratio of PLA to SPC (wt/wt) and ratio of MMC to SPC (wt/wt), volume ratio of oil phase to water phase chosen for the present investigation, were based on the results of preliminary experiments using a single-factor test; the emphasis of this paper was placed on the optimum production conditions and characterization of PLA–MMC–SPC nanoparticles in vitro.
Mitomycin C (MMC) (99.5%) was purchased from Shanghai Xin Ya Pharmaceutical Co. Ltd. PLA (Mw = 5000, 10000, 50000) were obtained from Shandong Medical Treatment and Instrument Institute. Soybean phosphatidylcholine was provided by Sigma Co. Ltd. Dichloromethane (DCM), dimethyl sulfoxide (DMSO), poly (vinyl alcohol) (PVA, degree of polymerization 1700, degree of hydrolysis 88.5%) used as a stabilizer in the external water phase were purchased from Xiamen Chemical Reagents Company (Xiamen, China). All other reagents and solvents were of analytical grade.
Preparation of MMC–SPC Complex
Due to both MMC and SPC being dispersed as the unimolecular form in DMSO solution, a waterless complex of MMC and SPC was formed after removal of the solvent. So the complex was prepared by an anhydrous co-solvent lyophilization method. Briefly, MMC powder and SPC with a ratio of 1:5 (wt/wt) were co-dissolved in dimethyl sulfoxide (DMSO) by gentle agitation. The resultant homogeneous solution was then freeze-dried overnight at a condenser temperature of −40 °C and under a vacuum of 10 Pa. So the MMC–SPC complex with a ratio of 1:5 was obtained; the MMC–SPC complex with a ratio of 1:10 and 3:10 (wt/wt) were also prepared in a same way used as the following optimal experiment.
The MMC–SPC physical mixture was prepared by mixing MMC with SPC (a ratio of 1:5 wt/wt).
FTIR Analysis of Complex
Fourier transform infrared spectrophotometry (FTIR Spectrometer, BRUKER IFS-55, Switzerland) was used to study the interaction between MMC and SPC. The FTIR spectra of MMC, SPC, the complex and physical mixture of MMC and SPC with a ratio of 1:5 (wt/wt) were obtained by the KBr method.
Solubilization Studies of Complex
Organic solvent dichloromethane (DCM) was used to evaluate the altered solubility of MMC after it was combined with SPC. Briefly, aliquots of organic solvent (2 mL) were introduced into MMC–SPC complexes (20 mg) and physical mixture (20 mg) of SPC and MMC with a ratio of 5:1, respectively, followed by gentle vortexing until an equilibrium system was obtained. The solubilization of each system before and after 24 h of storage was evaluated by visual examination.
Preparation of MMC–PLA–SPC Nanoparticles
MMC was formulated into PLA nanoparticles by a new single emulsion solvent evaporation method. Briefly, 6 mL DCM containing defined amounts of PLA was added to the MMC–SPC complex (60 mg), followed by gentle agitation until a micelle solution was obtained. The solution was poured into defined amounts of aqueous solution containing 0.25% PVA and then probe sonicated at 80 W for 5 s and repeated three times in an ice-water bath to form a stable o/w emulsion. After evaporation of the organic solvent with gentle stirring under atmospheric pressure for 24 h, the complex and polymer gradually co-precipitated in the emulsion droplets, so MMC–PLA–SPC nanoparticles were obtained. Those solidified nanoparticles were collected by ultracentrifugation, washed with distilled water three times, and lyophilized.
The drug entrapment efficiency (EE%) was determined indirectly by measuring the amount of free MMC using UV/vis spectrometer at 365 nm in the supernatant recovered after ultracentrifugation. The drug entrapment efficiency was expressed as percentage of the MMC difference between the initial amount of MMC and the free amount in the supernatant relative to the total amount used for the nanoparticles preparation.
To compare the results and those obtained by a classical method, the PLA–MMC microparticles were also prepared by a double emulation solvent evaporation method. The procedure for PLA–MMC microparticles was similar to the process mentioned above except that 6 mL DCM containing defined amounts of PLA was added to 3 mL of distilled water solution containing 10 mg MMC, and probe sonicated at 80 W for 5 s and repeated three times in an ice-water bath to form a w1/o primary emulsion, and followed by the w1/o emulsion droplets were poured into defined amounts of aqueous solution containing 0.25% PVA and homogenized at a rate of 1000 rpm.
Factor-level in orthogonal-design experiments of L9(34)
Characterization of PLA–MMC–SPC Nanoparticles
SEM (XL-30, Philips) was used to examine the surface morphology of PLA–MMC–SPC nanoparticles. The dried nanoparticles were mounted on metal stubs with double-sided electrical tape. They were gold coated under reduced pressure with a sputter coater before being viewed under the SEM at 20 kV. Zetasizer (Nano-ZS, Malven) was used to measure the size distribution and Zata potential of PLA–MMC nanoparticles. Prior to analysis, 10 mL of distilled water was added to a 20 mL vial containing PLA–MMC–SPC nanoparticles powder (containing 10 mg), and the vial was shaken. The characterization of PLA–MMC microparticles prepared by classical method was also examined in the same way as used for comparison.
Assay of In Vitro Drug Release
The in vitro release of MMC from the PLA–MMC–SPC nanoparticles was measured in PBS at pH 7.2. PLA–MMC–SPC nanoparticles weighing 40 mg were added in 50 mL of the medium in 60 mL conical screw capped tubes, preserved with 0.05% (w/v) sodium azide to prevent microbial growth. The samples were incubated at 37 °C and shaken horizontally at 100 cpm in a shaking incubator. At given time intervals, samples were removed from the vials tubes for quantitative estimation of the amount of drug released. In a typical test, 0.5 mL of the drug containing buffer solution was removed and the vial was replenished with 0.5 mL of fresh buffer solution to maintain a constant volume of the released medium. All release tests were run in triplicates.
The release of MMC from PLA–MMC microparticles was also measured in the same way as used for comparison.
Results and Discussion
Result of orthogonal-design experiments L9(34)
The zeta potential value (−42.2 mV) observed for PLA–MMC–SPC nanoparticles is significantly lower than −30 mV, the typical threshold value for flocculation , suggesting the suspension shows well stability, while zeta potential value for the PLA–MMC microparticles is found to be −12.6 mV. This significant difference of zeta potential value between PLA–MMC–SPC nanoparticles and PLA–MMC microparticles can be explained by the fact that SPC is an amphiphile and can be served as a surfactant; there was a minimal free SPC on their surface with hydrophilic head group of SPC toward the suspending medium during the formation of PLA–MMC–SPC nanoparticles.
This work demonstrates that the new single emulsion solvent evaporation method for the encapsulation of MMC in PLA nanoparticles results in improved formulation characteristics including smaller size, lower size distribution, higher encapsulation yield, and longer sustained drug release in comparison to classical method. The PLA–MMC–SPC nanoparticles system has a potential for long sustained delivery of MMC for local administration especially at tumor tissues and efficacy studies with these systems are underway.
This work was supported by the National Basic Research Program of China (2006CB933300) and the National Key Technology R&D Program (2007BAD07B05).
- Rauth AM, Mohindra JK, Tannock IF: Cancer Res.. 1983, 43: 4154. Google Scholar
- Rockwell S, Hughes CS: Cell Prolif.. 1994, 27: 153. COI number [1:CAS:528:DyaK2cXkvF2itbg%3D] 10.1111/j.1365-2184.1994.tb01413.xView ArticleGoogle Scholar
- Cummings J, Allan L, Smyth JF: Biochem. Pharmacol.. 1994, 47: 1345. COI number [1:CAS:528:DyaK2cXjtlSqurk%3D] 10.1016/0006-2952(94)90333-6View ArticleGoogle Scholar
- Nomura T, Saikawa A, Morita S, Sakaeda T, Yamashita F, Honda K: J. Control. Release. 1998, 52: 239. 10.1016/S0168-3659(97)00185-5View ArticleGoogle Scholar
- Richard YC, Yuming Y, Andrew MR, Norman M: Biomaterials. 2005, 26: 5375. 10.1016/j.biomaterials.2005.01.050View ArticleGoogle Scholar
- Ishiki N, Onishi H, Machida Y: Int. J. Pharm.. 2004, 279: 81. COI number [1:CAS:528:DC%2BD2cXltlygu7w%3D] 10.1016/j.ijpharm.2004.04.017View ArticleGoogle Scholar
- Onishi H, Takahashi H, Yoshiyasu M, Machida Y: Drug Dev. Ind. Pharm.. 2001, 27: 659. COI number [1:CAS:528:DC%2BD3MXotFaksrw%3D] 10.1081/DDC-100107322View ArticleGoogle Scholar
- Liu Y, Li H, Shu XZ, Gray SD, Prestwich GD: Fertil. Steril.. 2005, 83: 1275. COI number [1:CAS:528:DC%2BD2MXktFaru70%3D] 10.1016/j.fertnstert.2004.09.038View ArticleGoogle Scholar
- Yang XX, Chen JH, Liu ST, Guo D, Zeng XX: Regul. Toxicol. Pharmacol.. 2006, 46: 211. COI number [1:CAS:528:DC%2BD28Xht1Shu7nE] 10.1016/j.yrtph.2006.07.008View ArticleGoogle Scholar
- Sarısözen C, Aktaş Y, Mungan A, Bilensoy E: Eur. J. Pharm. Sci.. 2007, 32: S36. 10.1016/j.ejps.2007.05.076View ArticleGoogle Scholar
- Benita S, Benoit JP, Puisieux F, Thies C: J. Pharm. Sci.. 1984, 73: 1721. COI number [1:CAS:528:DyaL2MXhtlOlt7s%3D] 10.1002/jps.2600731215View ArticleGoogle Scholar
- Webb PA: Analytical Methods in Fine Particle Technology. Micromeritics Instrument Corporation, Norcross, GA; 1997:279.Google Scholar