60646449 blood

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molecular architecture and the structure of polymer/DNA complexes formed [3].

Amphiphilic block copolymers composed of hy-drophilic and hydrophobic segments can form a micel-lar structure with a hydrophobic compact inner core and a hydrophilic swollen outer shell in selective solvents, which is thermodynamically favorable for one block but unfavorable for the others [4]. These micelles are an in-teresting group of self-assembled nanocarriers for drug delivery, owing to the prospects of biocompatibility and large solubilization capacity for poorly watersoluble molecules. Poly(ethylene glycol)-b- poly( ε -caprolactone) (PCL-b-PEG) and poly(ethylene glycol)-b-poly(L-lactide) (PLL-b-PEG) diblock copolymers are very promising due to their stability and biocompatibility. Micelles formed of these copolymers have been utilized in encapsulation of different lipophilic drugs [5]. Note that it is also pos-sible to prepare nanocapsules or nanoparticles from these diblock copolymers in drug or active agent delivery. In

Potential c-myc Antisense Oligonucleotide Carriers: PCl/PEG/PEI and PLL/PEG/PEI

Sevil Din ç er Y ı ld ı z Technical University, Bioengineering Department, Davutpasa, Istanbul, Turkey

Mustafa T ü rk K ı r ı kkale University, Department of Biology, Yah s ihan, K ı r ı kkale, Turkey

Ay s e Karag ö z and G ü rhan Uzunalan Y ı ld ı z Technical University, Bioengineering Department, Davutpasa, Istanbul, Turkey

Abstract: In this work, positively charged, micelle-forming polymers were synthesized and used as a model vector to deliver antisense oligodeoxynucleotide (ASODN) into melanoma cells. Polymers and polymer/ASODN complexes were characterized by DLS according to size, charge, and critical micelle concentration. Nanosize and spherical complexes were observed by AFM. Complexes did not reveal signifi cant toxicity to melanoma cells. Antiproliferative effect of the complexes was observed by immunocytochemical staining and estimated as 56.8% with N/P:9. High amount of apoptosis and very small amount of necrosis were estimated. According to the results, these positively charged polymers forming micelle-like structures seem promising as ASODN carriers.

Keywords: antisense oligonucleotide , non-viral vectors , c-myc , poly(lactide) , poly(caprolactone) , poly(ethylene glycol) , polyethylenemine , micelle

INTRODUCTION

Gene delivery has great potential to cure many genetic and acquired diseases. Non-viral gene delivery is espe-cially advantageous because it could avoid unaccept-able immune responses. Various cationic polymers have shown promising effects in facilitating gene delivery as they readily complex with DNA to form polyplexes by neutralizing the negatively-charged anionic phosphate groups and hence improve transfection. Poly(ethylene imine) (PEI) is able to effectively complex even large DNA molecules [1,2], leading to homogeneous spherical particles with a size of 100 nm or less that are capable of transfecting cells effi ciently in vivo as well as in vitro . It offers a signifi cantly more effi cient protec tion against nuclease degradation than other polycations, e.g. poly(L-lysine), possibly due to their higher charge density and more effi cient complexation. However, further research is needed to rationalize the relationship between polymeric

This study was supported fi nancially by TUBITAK- 107T864. We thank Res. Asist. Yeliz Ba s aran for AFM images, and Res. Asist. Eray Dalgak ı ran for DLS analysis.

Address correspondence to S. Dincer, Bioengineering Department, Yildiz Technical University, Davutpasa, Istanbul, Turkey. E-mail: [email protected]

Artifi cial Cells, Blood Substitutes, and Biotechnology, 39: 143–154Copyright © 2011 Informa Healthcare USA, Inc.ISSN: 1073-1199 print / 1532-4184 onlineDOI: 10.3109/10731199.2010.506852

144 S. Dinçer et al.

Chang et al. ’ s study, PEG-PLA in the form of ultrathin membrane nanocapsules (80–150 nm) prepared as red blood cell (rbc) substitutes containing hemoglobin (Hb) and enzymes were reported [6].

Copolymers formed between cationic polymers such as PEI and the aforementioned diblock copolymers offer the benefi t of electrostatic complexation while enhanc-ing solubility and stability of the polyplexes. Insertion of hydrophilic segments (PEG) into diblock copolymers provides a hydrophilic corona that creates a steric bar-rier against self-aggregation, shielding of cationic charge groups, and inhibits the association with plasma proteins and other cellular components. Moon et al. [7] described the synthesis of diblock, triblock, and 4 arm star-shaped block PEG – PTMC copolymers and the characteristics of micelle as a potential drug delivery vehicle. Addition of a positively charged unit to these copolymers can allow their use as gene delivery vehicles.

ASODNs can either hybridize with specifi c mRNA, which would inhibit the transcription of genetic informa-tion into protein synthesis, or activate the RNase H that can digest the mRNA resulting in the pathway blockage. These oligonucelotides targeted to oncogenes are widely used in order to provide specifi c and effective means to prevent the growth of cancer cells. c- myc , a member of the myc gene family, is a key regulator of cell growth that has been found altered by amplifi cation or point mu-tation in a large subset of tumors, including leukemia, melanoma, prostate, breast, and colon carcinomas [8,9]. The effi cacy of these oligonucleotides in inhibiting gene expression depends on their ability to penetrate targeted cells. The uptake of them occurs through active transport, which, in turn, depends on the temperature, the structure, and the concentration [10]. Several approaches have been explored to enhance cellular uptake and permeability in order to increase their therapeutic effi cacy, including con-jugation to polycations, targeting cell surface receptors, coupling to cholesterol, and encapsulation into lipid parti-cles such as microspheres and liposomes. The use of vec-tors in antisense drug delivery in vivo seems to improve their biological effects.

Growth inhibition of SK-MEL-30 human melanoma cells by antisense c-myc oligonucleotides delivered by poly(N-Isopropylacrylamide)/poly(ethyleneimine) copo-lymer was reported by our group. By this polymer, we have only investigated the c-myc inhibition by MTT as-say [11]. In this study, we have reported the synthesis and characterization of PEI coupled PCL-mPEG and PLL-mPEG diblock copolymers having the ability to form mi-celle-type structures for potential use in delivery of c- myc antisense oligonucleotide to melanoma cells. All poly-mers were investigated by Zeta Sizer for their size and charge characteristics. Protonation ability of polymers was followed by this technique using different pH values. Also, complexation ability of ASODNs with prepared

positively charged polymers was investigated by measur-ing their sizes and charges in different N/P ratios. AFM was also used to examine the corresponding micelle-type structures. After physicochemical characterization of polymer ASODN complexes, we have investigated the c-myc inhibition effi ciency of these complexes. Apoptosis and necrosis indexes were evaluated. Results showed that these particular carriers would be potential candidates in the uptake of oligonucleotides to melanoma cells.

MATERIALS AND METHODS

Materials

Methoxy poly(ethylene glycol) (Mn: 5000, Fluka, Germa-ny; Mn: 2000, Sigma-Aldrich, Germany), poly(ethylene glycol) (PEG, Mn: 2000 and 5000 Sigma-Aldrich, Ger-many), ε -caprolactone ( ε -CL, Aldrich, USA), stannous octoate ((SnOct 2 ), Sigma, USA), diethyl ether, chloroform, and dichloromethane were used as received. L-Lactide (Aldrich, USA) was recrystallized with toluene. Branched polyethyleneimine (PEI, MW: 2000, Aldrich, Germany) was used as received. Carbonyldiimidazole (CDI) was obtained from Sigma (Germany). TNBS (2,4,6-trini-trobenzene sulfonic acid) and pyrene were purhased from Sigma-Aldrich (Germany). A 15-mer AS ODN (5 ’ -AACGTTGAGGGGCAT-3 ’ ) that was complemen-tary to the translation initiation region of c-myc oncogene was obtained from Iontek Ltd. (Turkey) and used in all experiments. Purity was � 95% provided by high perfor-mance liquid chromatograpy.

Methods

Preparation of positively charged PCL-mPEG and PLL-mPEG diblock copolymers . PCL-mPEG and PLL-mPEG diblock copolymers carrying two different methoxy PEG molecules (Mn: 2000 and 5000) were prepared by mi-crowave irradiaton using Milestone S.r.l MicroSYNTH microwave synthesis unit. Details for synthesis and char-acterization were reported elsewhere [12]. For the prepa-ration of PEI-carrying polymers, diblock copolymers (PCL-mPEG, PLL-mPEG) in 4:1 ratio were used because of their water solubility. In the coupling procedure carbo-nyldiimidazole was used to activate the hydroxyl group of polymers. The polymer sample was dissolved in di-oxane in a concentration of 8 � 10 �3 M. Then, 0.08 M CDI was added to the medium and the reaction mixture was stirred for 3 h at 37 o C. At the end of the reaction, the mixture was precipitated from diethyl ether. This procedure was repeated three times and the obtained product was dried in vacuum overnight. Coupling of the activated polymer to the PEI by amino groups was then

Antisense Oligonucleotide Carriers 145

performed. CDI-activated polymer was dissolved in bo-rate buffer (pH:8.5) and PEI (2000, branched) was added to the medium in 1:1 ratio (mole). The reaction mixture was incubated at room temperature for 24 h. Unreacted polymers were removed using an ultrafi ltration system (Millipore) by taking into account the molecular weight of corresponding polymers as reported elsewhere [12]. The product was liophilized for further use.

TNBS assay. In gene delivery applications, the compl-exation of polymer and genetic material (here, oligo-nucleotide) depends on the amount of amino groups of polymer and phosphate groups of ODN. It is not possible to know the exact amount of amino groups of branched PEI (MW: 2000) molecule used here. Therefore, there is a need to estimate the amount of primary amine groups for complexation studies. Amino-group content of PEI-bound polymers was investigated by the TNBS (2,4,6-trinitroben-zene sulfonic acid) method [13]. To do this, a calibration curve was obtained using glycine amino acid in different concentrations (0.5, 0.1, 0.05, 0.01, 0.001 mg/ml) at pH: 8.5. TNBS was added in a ratio of 0.1% and the reaction mixture was incubated at 40 o C for 2 h. Following incuba-tion, each sample was measured at 335 nm by UV-Visible Spectrophotometer and recorded. Amine group content of each polymer was estimated from the calibration curve. In addition to this method, gel permeation chromatography (GPC) was also used to confi rm polymer formation by using PEG as standard.

Preparation of polymer/ASODN complexes . Stock solu-tions of ODN (5.68.10 �6 M) and polymer (1 mg/ml) were prepared in a phosphate buffer. Complexes were prepared by adding ASODN solution to the polymer solution in de-sired amounts to achieve different N/P ratios. Here, poly-mer amounts were used according to their amine content estimated by TNBS assay. After mixing of ASODN and polymer with mild shaking, the sample was left at room temperature for 30 min to equilibrate before use.

Dynamic Light Scattering (DLS) . DLS measures the in-tensity correlation function of light scattered from a poly-meric solution. All DLS measurements were performed using a Malvern Instruments NanoS Nanosizer. Samples analyzed were contained in a 1 cm-path length cell, and the data were analyzed using Malvern Instruments Dis-persion Technology Software. The polymer refractive index was taken to be 1.5 with an absorbance of 0.01. The viscosity and refractive index of water were taken as 0.8877 cPa and 1.330, respectively. Six measurements were performed on each sample, with an average of 10 runs taken for each measurement, each within 1 min. We have estimated the critical micelle concentration by using data obtained by this instrument. In addition, changes in zeta potentials and sizes of PEI-coupled polymers were

evaluated in different pHs. Polymer/ASODN interaction was followed by the same instrument in different N/P ratios at physiological pH.

Atomic Force Microscopy (AFM). Complex solutions were deposited onto freshly cleaved mica surfaces and dried at room temperature for 5 min. The images were observed by Tapping Mode using the AFM microscope (SPM9600, Shimadzu, Japan) with 10 nm silicon nitride tips. Analysis was performed to investigate the size and images of selected polymers and ASODN complexes.

Cell Culture . SK-MEL30 melanoma cells were obtained from Hacettepe University, Biochemistry Department. The cells were cultured in Dulbecco ’ s Modifi ed Medium without L-glutamine (DMEM, Sigma, Germany) supple-mented 10% Fetal Bovine Serum (FBS, Sigma, Germany), and 1% penicilin-streptomycin (Sigma, Germany) at 37 o C and 5% CO 2 atmosphere. The cells were subcultured twice a week, using dissocation medium, trypsin-EDTA, pH 7,4 as buffer system. All tests were triplicated. Statistical sig-nifi cance of diferences between test values was estimated using Nonparametric Kruskal-Wallis test. p � 0.1.

MTT assay . For MTT experiments, cells were cultured in 96-well plates at a density of 5 � 10 3 per well and grown overnight at 37 o C, 5% CO 2 atmosphere. The cell culture medium was removed and then replaced. Copolymer/ASODN complexes formed at different N/P ratios were added into each well. Cells were incubated for 72 h. MTT reagent (5 mg/ml) was added into each well, and the cells were cultured for a further 4h incubation. After that, 100 μ l 10% sodium dodecyl sulfate (in 0.01 N HCl) were added to each well and incubated overnight. Then, plates were read in Elisa Microplate Reader at 570 nm. Dark blue formazan crystals are formed if the cells are alive.

Cell transfection . Cells were seeded on cover glasses in 6 well plates at a density of 10 � 10 3 per well and grown overnight at 37 ° C, 5% CO 2 atmosphere. The cell medium was removed and washed with PBS three times. After polymer/ASODN complexes formed at N/P ratio: 1, 3, 6, and 9 were added into each well for 24 hours. Only ASODN was used as a control.

Immunocytochemical detection of c-myc expression in cell culture . SK-MEL 30 human melanoma cells (10�10 3 cells per well) were placed on cover glasses in DMEM with-out L-glutamine in 6-well plates and incubated at 37 ° C in 5% CO 2 atmosphere. Then these cells were washed with distilled water and polymer/ASODN complexes in dif-ferent N/P ratio (1, 3, 6, and 9) were applied to cells for 24 hours. Following that, slides stained for c-myc antigen were cytocentrifuged, fi xed in cold acetone at −20 o C for 10 minutes, and treated with hydrogen peroxide (0.3% in


methanol) for 10 min to block the endogenous peroxidase activity. Then they were washed in PBS and incubated with c-myc antibody (Santa Cruz, 1:100 dilution) at room temperature for 1 h. As a negative control, preimmune mouse serum, instead of primary antibody, was used. For immunohistochemical demonstration of the c-myc protein, an avidin-biotin-peroxidase technique was used [14]. The peroxidase-antiperoxidase technique [15] was used to demonstrate the c-erbB-2 protein. The immu-noreactivity of the c-myc antibody was confi ned to the cytoplasm and nuclear of SKMEL-30 cells. We counted the number of c-myc positive cytoplasmic and nuclear staining cells in all fi elds found at 400 � fi nal magnifi ca-tion. c-myc positive cells were seen to be brown under a light microscope. For each slide, three randomly selected microscopic fi elds were observed and at least 1000 cells/fi eld were evaluated.

Analysis of apoptosis and necrosis . Double staining was performed to quantify the number of apoptotic cells in the culture, based on scoring apoptotic cell nuclei. SKMEL-30 cells (20 � 10 3 cells per well) were placed in DMEM us-ing 24-well plates. After treating with polymer/ASODN complex at N/P ratio of 1,3,6 and 9 (in aqueous solutions) for a 24- hour period, both attached and detached cells were collected, washed with PBS, and then stained with Hoechst dye 33342 (2 μ g/mL), propodium iodide (PI) (1 μ g/mL) and DNAse free-RNAse (100 μ g/mL) for 15 min at room temperature. Then, 10–50 μ L of cell suspension was smeared on the slide and cover slip for examination using fl uorescence microscopy. In addition, attached cells were washed with PBS and stained in plates in the same manner. While the nuclei of normal cells were stained light blue, apoptotic cells were stained bright blue by the Hoechst dye. The apoptotic cells, from their nuclear morphology, were identifi ed as a nuclear fragmentation or chromatin condensation. Necrotic cells were stained red by PI. Necrotic cells lacking plasma membrane integrity allow PI dye to cross the cell membrane, meaning that PI dye does not cross the non-necrotic cell membrane. The results of the counted number of apoptotic and necrotic cells in 10 randomly chosen microscopic fi elds were expressed as a ratio of apoptotic and necrotic to normal cells. The number of apoptotic and necrotic cells were determined by Fluorescence Inverted Microscope (Leica, Germany) using DAPI and FITC fi lters.

RESULTS

Polymer Characterization

As mentioned in earlier, PCL-mPEG and PLL-mPEG diblock copolymers were synthesized by microwave irradiaton and polymer fromation was confi rmed by FTIR

and 1 H-NMR. Molecular weight data were obtained from GPC and also 1 H-NMR spectra. All data were reported else-where [12]. Here, we have prepared the PEI-bound form of these diblock copolymers. After a series of purfi cation steps by ultrafi ltration, pure PEI-bound polymers were obtained and characterized by different techniques. Addition of PEI into the diblock copolymer structure was confi rmed by TNBS assay and GPC as explained below.

Figure 1 shows representative unimodal GPC traces of PCLPEG5000 and PCLPEG5000/PEI. The addition of PEI to the diblock copolymer caused higher molecular weight value as seen here and the obtained polymers after PEI conjugation seem close to monodispersitiy.

Determination of Amino-group Content

The PEI molecule used in this study has a branched struc-ture containing tertiary, secondary, and primary-amino groups, which are not easy to determine with direct meth-ods. It is important to estimate the amino content of the corresponding polymers since the quantity of especially primary amino-groups is required for the complexation with genetic material by electrostatic interaction. Here, we have performed TNBS assay and obtained approxi-mate values. Each sample reacted with TNBS was mea-sured at 335 nm by UV-Visible Spectrophotometer and amine group content of each polymer was estimated from the calibration curve (y � 12816x � 0.3117, R 2 � 0.9871). In this way, the success of PEI-coupling to polymers was also demonstrated. Amine content of each polymer was obtained as 0.14, 0.10, 0.15, 0.15 mg/ml for PCL-mPEG2000/PEI, PCL-mPEG5000/PEI, PLL-mPEG2000/PEI, PLL-mPEG5000/PEI, respectively.

Figure 1. GPC chromatograms of PCLPEG5000 and PCLPEG5000/PEI.


Light Scattering Measurements

The charge and size of the polymer has great infl uence on the stability, DNA-binding, and release effi ciency of polyplexes, and thus on targeting effi ciency. Several stud-ies reported the importance of positive charge of different polymers to be used in gene delivery [1–3,19–22].

DLS detects the mean dimension of particles in aquous soluiton based on the Stocks-Einstein equation. Measurements were made for positively charged diblock copolymers and polymer/ASODN conjugates.

Determination of cmc . As explained in the Methods sec-tion, the micelle forming ability of PCL-mPEG and PLL-mPEG diblock copolymers and their PEI-bound forms were investigated by a Zeta Sizer. Figure 2 shows inten-sity vs. concentration curves of diblock copolymers. Up to a certain concentration value (0.05 mg/ml), intensity did not reveal any signifi cant increase; however, after this value, a sharp increase in intensity was observed for all polymers. This certain concentration can be accepted as criticial micelle concentration ( cmc ) [16]. Note that by this concentration value a remarkable decrease in size was also observed, probably caused by ordered micelle structure formation. This increase was observed for lactide-based copolymers, which meant that miscellar structure forms more easily with these polymers. Addi-tion of PEI to the diblock copolymer structure did not affect very much the micelle formation for each of the polymers. Micelle formation is expected to be easy for diblock copolymers since there is only one hydrophilic and one hydrophobic block. In the PEI-bound case, the to-tal polymer chain posseses two hydrophilic chains in both ends and one hydrophobic in the middle. Therefore, a mi-celle formation may be suggested, as in Scheme 1. We did not obtain very different cmc values because all diblock

copolymers and their PEI-bound forms do not possess dif-ferent structures in terms of hidrophobic and hydrophilic balance. For the PEI-bound polymers, the concentration was not different form 0.05 mg/ml. Zhang et al. reported the CMCs of poly(D,L- Lactide)-b-mPEG copolymers in the range of 3.5–0.5 mg/L changing by PDLLA length in the polymer chain [17]. Gyun et al. found CMC of meth-oxy propyleneglycol/caprolactone micelles as between 3.47–0.63.10 � 7 mol/lt [4].

Size and charge characterization of PEI-coupled diblock copolymers . The following results can be drawn from size and charge analyses: For diblock copolymer, PCL-mPEG2000, size was determined as 138 nm without PEI. Size of PEI-including copolymer ( PCL-mPEG2000-PEI) at pH: 2 and 10 were determined as 89 and 204 nm, re-spectively (Figure 3). However, at pH:7.4, the size of this polymer was 184 nm. By increasing pH, PEI units (especially between pH: 2–8) become protonated and start to swell (proton sponge effect), and this causes an increase in the hydrodynamic size of the polymer. This

Figure 2. Change in intensity by diblock copolymers con-centration.

Scheme 1. Micelle formation of PEI-bound diblock copolymers.

Figure 3. Change in size of PEI-bound polymers by pH.


behaviour does not occur after pH: 8, which is the up-per pKa value of PEI. Charge of this polymer was also evaluated (Figure 4). At acidic pHs, the polymer gained a positive charge as expected ( � 6.57 at pH:2 and � 13,17 at pH: 4), since PEI has a great protonation capacity in acidic medium towards even higher pH values ( � 16.8 at pH: 7.4 and ( � 16.1 at pH: 8) [1]. However, at very basic medium (such as pH: 10), the polymer was not positively charged any more (close to zero).

For PCL-mPEG5000-PEI , while size was 100 and 195 nm at pH:2 and 10, respectively, it was 175 nm at pH:7.4. The size of the diblock form of this polymer was 176 nm at pH:7.4, proving no negative effect on particle formation of PEI-additon to the structure. This poly-mer has similar behavior to PCL-mPEG2000PEI hav-ing smaller size and charge in lower pH values. It was positively charged until pH: 8 ( � 10.2), but negatively charged after this pH (−2.38 at pH: 10). PLL-mPEG2000-PEI was positively charged until pH:7.4 ( � 4.86, � 24.6, � 14.1, � 18.8 at pH: 2, 4, 7, 7.4, respectively), but nega-tively charged at pH: 10 (−8.29). Size increased to 163 nm (at pH: 7.4); after that, this increase reached up to 336 nm at pH: 10, probably caused by aggregation. The size of the diblock form of this polymer was 137 nm at pH:7.4, which is little different from PEI-bound from (163 nm). PLL-mPEG5000-PEI was positively charged until pH:7.4 ( � 4.87, � 16.6, � 16.5, � 18.3 at pH: 2, 4, 7.4, 8), but negatively charged at pH 10 (-8.41). Size was 162 nm at pH: 7.4, whereas it was 111, 109, 163 and 235 nm at pH: 2, 4, 8 and 10, respectively. This revealed that good micelle formation was achieved at physiological pH. Note that the size of PLL-mPEG5000 was 154 nm. The particle sizes of all polymers were in a similar range. Measured sizes here are probably much higher than the original value because the Zeta Sizer instrument mea-sures the hydrodynamic size of the particles. PEI addition to the polymer structure was confi rmed by these analyses. It was also demonstrated that the PEI molecule had high

protonation capacity, which makes PEI very attractive as an effi cient gene delivery vector [1,2].

Polymer/ASODN conjugates . For size and charge of polymer/ASODN conjugates, polyplexes were prepared in different N/P ratios (1, 3, 6, 9) by taking into account the amino con-tent calculated from TNBS analysis. All polymers revealed sizes in a similar range because of the similarity of resulting structures. According to Table 1 (PCL-mPEG2000-PEI/ASODN), mixing of ODN leads to a small increase in the diameter (polymer ’ s diameter was 184 nm). As the concen-tration of polymer increases (increase in N/P ratio), the size of polyplexes decreased to 120 nm (at N/P:9). Thus, N/P:6 seems the best ratio for good complexation because of the smallest polydispersity. This can be seen also from Figure 5, representing volume intensity distribution profi les plotted against hydrodynamic diameters. Note that size is not the only determinant in effi cient transfection.

PCL-mPEG5000-PEI/ASODN : charge of polymer showed a similar trend with the previous polymer sample. Here, the smallest complex size ( ∼ 140 nm) was obtained at N/P:6 and 9, in which polyplexes had an extra positve charge ( � 4–5 mV). PLL-mPEG2000-PEI/ASODN : in-creasing of size by N:P ratio may cause aggregation of complexes, so that up to N:P:6 seems effi cient enough. At this ratio, complex has extra surface charge. PLL-mPEG5000-PEI/ASODN : size of polyplexes increased up to N/P: 6. N/P: 9 seems the best ratio at which size is smallest and charge is highest.

Atomic Force Microscopy (AFM)

Figure 6 shows SPM image of PCL-mPEG2000/PEI/ASODN complexes in different N/P ratios. Complexes were prepared by adding ODN solution to the polymer

Table 1. Charge and size of polymer/ASODN complexes measured by DLS in different N/P ratios.

Polymer N:P Charge (mV) Size (nm)

PCL-mPEG2000/PEI 1369

1.97 � 0.34.10 � 0.75.35 � 1.26.71 � 1.7

212 � 15204 � 25195 � 8123 � 5

PCL-mPEG5000/PEI 1369

1.51 � 0.64.76 � 0.55.37 � 1.14.12 � 2.3

155 � 20145 � 20155 � 15145 � 5

PLL-mPEG2000/PEI 1369

1.25 � 0.81.83 � 0.94.60 � 1.64.75 � 2.5

292 � 15294 � 30242 � 10250 � 10

PLL-mPEG5000/PEI 1369

2.15 � 0.5 5.83 � 0.94.48 � 1.44.52 � 1.6

180 � 12137 � 10248 � 13209 � 2

Figure 4. Change in charge of PEI-bound polymers with pH.


solution in desired amounts to achieve different N/P ra-tios. After mixing of ASODN, the sample was left at room temperature for 30 min to equilibrate before use. Sapmles were dropped onto freshly celaved mica and dried at room temperature. As clearly seen here, complexes formed spherical particles, which can be supposed to be micelle. In some regions, a kind of aggregates were formed, which can be overcome by preparation of more diluted sample. However, in all ratios very small structures were obtained (between 10–30nm). More uniform particles were formed in N/P ratio of 6. In N/P:1, very small particles were obtained but at the same time they seemed to have a ten-dency to be aggregated. In N/P ratio 1 and 9, more poly-dispersity was observed comparing to N/P: 6, as also seen in DLS profi les (Figure 5). The size observed by AFM seems inconsistent with the ones obtained by DLS, but this was expected since the DLS instrument measures the hydrodynamic volume of the sample. The results showed that formation of spherical structures obtained by polymer alone was not affected in the presence of ASODN.

MTT Assay

ASODN did not reveal any toxicity towards SKMEL-30 cells. Polymers (100 μ M) without ASODN showed tox-icities caused by positive charge on the polymer surface. Cell viability after polymer/ASODN transfection was ob-tained as seen in Figure 7 While positive charge enhanced toxicity directly, size increase did not affect this as much as charge. MTT assay of polymer/ASODN complexes depending on time was also evaluated. No signifi cant difference was observed in cell viability between 48 and 72 hour incubation time. Similar results were obtained for the poly(N-Isopropylacrylamide)/poly(ethyleneimine) complexed with the same ASODN in terms of polymer toxicity and incubation time [11].

Cell Transfection by Polymer/ASODN Complexes and c-myc Expression

c-myc expression was followed by immunocytochemical staining, as mentioned earlier. Polymer/ASODN complex-es in different N/P ratios were transfected into SKMEL-30 cells seeded on cover glass. Naked oligonucletide was used as a control and revealed only 5% c-myc inhibition. By the polymers without ASODN cell inhibition was also observed (4.3–7.7%), but this was most likely because of the toxic effect of unoccupied positively charged polymer chains. Results are shown in Table 2 and c-myc activites are illustrated in Figure 8. Most of the complexes showed a certain amount of cell inhibition as seen in Table 2. As pre-viously reported in several studies, transfection effi ciency decreased with decreasing positive charge density [3]. In the low N/P ratio range, it is expected that some of the ASODNs are not complexed with polymer. That means complexes are not going to be formed and therefore this will cause reduced transfection. Zhao et al. reported that lowering the N/P ratio to below 1 resulted in lower trans-fection effi ciency [18].

Figure 6. AFM images of PCL-mPEG2000-PEI/ASODN complexes at different N/P ratios (1, 6, 9).

Figure 5. Light scattering profi les of PCL-mPEG2000-PEI/ASODN complexes at different N/P ratios (1, 3, 6, 9).


Figure 8A shows c-myc positive cells seen as brown spots transfected with only naked oligonucleotide. The following images were taken after transfection by the complexes formed between polymers and ASODN. As seen in these images, complex formation caused lower c-myc activity, especially at lower N/P ratios and higher particle sizes. The decrease in complex size and increase in complex charge allowed enhanced oligo uptake into the cells; therefore inhibited c-myc activity was seen as blue spots in the Figure 8B. It seems that the charge of the complexes is more effective on the c-myc expression more than size difference. Most of the complexes actually are in a similar size range especially seen in AFM images. c-myc expression was inhibited as 56.8% and 49.1% with transfection by PCL-mPEG2000/PEI in N/P: 9 and PLL-mPEG2000/PEI in N/P: 3, respectively (Figure 8B and D). When the complex charge reached a very high value, toxicity was observed. Polymers without oligonucleotide revealed a similar trend with the control group.

Apoptotic and Necrotic Effect of Complexes

Apoptosis results are in a consistency with c-myc activ-ity. Apoptotic cell ratio was obtained as 3% and this

ratio was increased by transfection of polymer/ASODN complexes depending on the charge and particle sizes (Table 3). As seen in the control experiment, all of the cell nuclei were stained by Hoechst 33342 as light blue representing non-apoptotic cells (Figure 9A). Polymer/ASODN complexes caused apoptosis as seen in bright blue spots (Figure 9B). The highest apoptotic effect was observed in high N/P ratios. This might be because of the free positive charge on the complex facilitating cell entrance and endosomal escape. For most of the poly-mers, N/P: 9 seems a good ratio for the effi ciency. Al-though toxicity of the polymers without oligonucleotide were increased by size and charge, apoptotic effect was observed in lower values. Apoptosis results seem in con-sistency with MTT assay.

In the necrotic effect study, naked ASODN did not cause necrosis; however, 100 μ M polymers revealed in be-tween 10%–15% necrosis. Complexation between poly-mer/ASODN affected necrosis in a way that was increased by the N/P ratio and therefore by the charge of the com-plexes. As seen in Figure 9D, the higher the positive charge, the more necrotic cells were obtained. Necrotic cells ap-peared in red (PLL-mPEG2000/PEI/ASODN complex at N/P:9), while the others were in green (stained by Hoechst 33342). Figure 9C represents the control group not con-taining polymers and appears in green.

DISCUSSION

This study reported the use of PEI-coupled PCL-mPEG and PLL-mPEG diblock copolymers in ASODN delivery to SKMEL-30 cells. Diblock copolymers were synthesized by microwave irradiation and characterized as reported elsewhere [12]. Here, the PEI-bound form of these diblock copolymers was prepared and polymer formation was demonstrated by TNBS assay and GPC.

DLS was used to investigate the charge and size characteristics of polymers and also polymer/ASODN complexes. The micelle forming ability of PCL-mPEG and PLL-mPEG diblock copolymers and their PEI-bound forms was investigated by this technique and it was estimated that a sharp increase in intensity after 0.05 mg/ml was observed for all polymers, which can be accepted as cmc . It was observed that the charge of the polymers increased, especially in the acidic medium, be-cause of the great buffering capacity of the PEI molecule. Obtained micelle-like structures and complexes were con-fi rmed by DLS in terms of polydispersity and optimal N/P ratio was found as 6. AFM images of polymer/ASODN complexes showed that spherical structures were formed also in the presence of ASODN. However, the sizes of the corresponding structures were in the range of 10–30 nm, approximately, which were different from the ones obtained by DLS. This was because of the DLS technique

Figure 7. MTT assay of polymer/ASODN complexes depending on N/P ratio. Bars represent mean �3% S.D.

Table 2. c-myc expression index of SKMEL-30 cells obtained by immunocytochemistry staining method (p�0.071).

c-myc negative cell (%)

Polymer without ASODN

N/P ratio

1 3 6 9

PCL-mPEG2000/PEI 4.3 14.5 23.3 33.5 56.8PCL-mPEG5000/PEI 7.7 13.2 22.7 44.6 62.8PLL-mPEG2000/PEI 6.4 15.7 49.1 32.4 39.6PLL-mPEG5000/PEI 5.2 11.3 26.6 14.3 21.8


Figure 8. Immunocytochemistry images of stained SKMEL-30 cell with c-myc antibody. (A) Nucleus of cell (stained with c-myc antibody), where brown spots indicate c-myc positive cells as a control (non-treated with polymer/ASODN complex). (B) Cells transfected with PCL-mPEG5000/PEI at N/P: 9; blue spots show c-myc negative cells. (C) Cells transfected with PCL-mPEG2000/PEI at N/P: 9; arrow shows c-myc positive cells and some of cells nuclei blue as c-myc negative cell. (D) Cells transfected with PLL-mPEG2000/PEI at N/P: 3; arrow shows c-myc-positive cell. (E) Cells transfected with PCL-mPEG5000/PEI at N/P: 1; arrow showss c-myc positive cell. (F) Cells transfected with PLL-mPEG5000/PEI at N/P: 3; arrow shows c-myc positive cell. Images were recorded with � 400 magnifi cation and with an Olympus research microscopy.

measuring the hydrodynamic size of the resultant com-plexes that were higher than the original ones.

According to MTT assay, polymers not carrying ASODN showed some toxicity because of the free posi-tive charge of PEI. MTT assay for the polymer/ASODN complexes depending on charge and incubation time

was consistent with another study performed by poly(N-Isopropylacrylamide)/poly(ethyleneimine) [11].

Expression of c-myc was followed by immunocy-tochemical staining. Naked oligonucletide showed only 5% c-myc inhibition. A small amount of inhibiton (4.3–7.7%) was also observed for the polymers without


Figure 9. Fluorescence inverted microscopy image of SKMEL-30 carcinoma cells. (A) Nucleus of cells (stained with Hoescht 33342), where blue spots indicate nucleus of non-apoptotic cells as a control. (B) Shining and smashed nucleus (shown with arrow) of apoptotic cells in PCL-mPEG2000/PEI (N/P;9) containing medium. (C) Fluorescence microscopy image of cells (stained with Hoescht 33342), where formation of green cells demonstrates non-necrotic cells (photo taken under FITC fi lter) as a control. (D) Nucleus of SKMEL-30 cells (stained with PI and Hoescht 33342), where dense red spots indicate nucleus of necrotic cells and green cells indicate non-necrotic cells. Images were recorded with � 400 magnifi cation. Photos A and B were taken under DAPI fi lter and C and D taken under FITC fi lter.

Table 3. Apoptotic and necrotic indexes of SKMEL-30 carcinoma cells; result obtained with double staining method (p�0.085 for Apoptotic indexes, p�0.069 for Necrotic indexes).

Apoptotic index (%)* Necrotic index (%)*

N/P ratio 1 3 6 9 1 3 6 9

PCL-mPEG2000/PEI 17.5 26.3 32.4 40.8 5.4 11.3 20.6 25.8PCL-mPEG5000/PEI 18.7 29.2 37.6 52.3 3.2 7.6 10.9 19.6PLL-mPEG2000/PEI 18.1 43.7 38.8 36.5 18.3 23.6 16.4 32.7PLL-mPEG5000/PEI 13.4 22.6 9.7 19.8 9.4 13.7 5.6 12.7

*For naked ASODN apoptotic and necrotic indexes were 3 and 2%, respectively. Polymers without ASODN revealed apoptotic indexes as 4.3, 6.2, 8.6, 3.1, and necrotic indexes as 10.6, 18.2, 21.7, 8.9 for PCL-mPEG2000/PEI, PCL-mPEG5000/PEI, PLL-mPEG2000/PEI, PLL-mPEG5000/PEI, respectively.

ASODN, probably because of the toxicity related to positive charge. Most of the complexes showed a certain amount of cell inhibition, as seen Table 2. For example, c-myc inhibiton ratio was estimated as 56.8% and 49.1% with PCL-mPEG2000/PEI in N/P: 9 and PLL-mPEG2000/PEI in N/P: 3, respectively. For the effi cient inhibition,

lower N/P ratios did not seem as appropriate as the higher ones because of insuffi cient complex formation.

Several cationic polymers containing hydrophilic PEG blocks have been used as transfecting vectors for different genes [19–20]. In the case of PEI as a cationic part, the high transfecting effi ciencies observed have been attributed to


the strong buffering capacity under the physiological pH conditions. PEI buffers inside the endosomes due to the transfected polycations pump protons into the endosomes; this is called the proton sponge effect. This causes an in-crease in the osmotic pressure inside the endosome, which destabilizes the endosome, resulting in the escape of the gene complexes from the degradation inside the lysosomal environment.

Gebhart et al. [21] and Ochietti et al. [22] have re-ported that grafting of a hydrophobic polymeric block to a cationic PEI block can lead to the enhancement of transfection effi ciency and control of favorable biodis-tribution of the complexes in animal models. They have suggested that by tuning the amphiphilicity of copoly-mers the binding with gene molecules can be made more effective, resulting in a favorable size range of the nanop-olyplexes. They have also speculated that amphiphilicity together with the variation of block size would allow one to examine the effect of hydrophobic interaction on the nanostructure and net charge density of the oligonucle-otide polyplexes. The relationship between such informa-tion with cell transfection and cytotoxicity needs to be studied for more effi cient results [19].

In this study, c-myc activity was not demonstrated by only MTT and immunocytochemical staining. Apoptosis and necrosis indexes were also evaluated. Here, com-plexes caused apoptosis in the cells while it was obtained only 3% by the polymer alone. For most of the polymers, N/P: 9 seems a good ratio for the effi ciency. On the other hand, necrosis caused by the polymers increased by the N/P ratio depending on the unoccupied positively charged chains. It was concluded that the optimal N/P ratio has to be estimated in order not to cause necrosis but at the same time good apoptosis related to c-myc inhibition. Accord-ing to the results, the most effi cient N/P ratio seems to be between 6 and 9.

CONCLUSIONS

In this study we have prepared polymers and polymer/ASODN complexes and used DLS and AFM to charac-terize the size and charge characteristics. We have inves-tigated these propeties in different N/P ratios. After all, these complexes were evaluated by their c-myc activity towards SK-MEL 30 cells together with apoptotic and necrotic effect.

Since a very small oligonucleotide was used in this study, shrinkage of genetic material was not expected that much, which was in the case of using large DNA chains. DLS experiments showed that the N/P ratio affected the uniformity of the complexes, as also seen in AFM images. All polymers seem to have the ability of micelle forming as demonstrated by DLS and AFM. We obtained very small particles after complexation, but the most uniform ones

were obtained especially in N/P:6. The cell culture studies showed that N/P:9 was also accepable in terms of c-myc transfection and inhibition. Complexes showed apoptotic activity, while a small amount of necrotic behavior was observed, possibly because of positive charges. Since all polymers are similar in terms of structural properties, they did not reveal a great difference in corresponding inhi-bition activity. According to the results, these polymers seems to have a potential to improve intracellular avail-ability for c-myc directed antisense strategies.

Declaration of interest: The authors report no confl icts of interest. The authors alone are responsible for the content and writing of the paper.

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