Evaluation of cationic polyamidoamine dendrimers’ dermal toxicity in the rat skin model
Authors Winnicka K, Wroblewska M, Sosnowska K, Car H, Kasacka I
Received 30 November 2014
Accepted for publication 30 December 2014
Published 5 March 2015 Volume 2015:9 Pages 1367—1377
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Editor who approved publication: Professor Shu-Feng Zhou
Katarzyna Winnicka,1 Magdalena Wroblewska,1 Katarzyna Sosnowska,1 Halina Car,2 Irena Kasacka3
1Department of Pharmaceutical Technology, Faculty of Pharmacy, Medical University of Bialystok, Bialystok, Poland; 2Department of Experimental Pharmacology, Faculty of Health Sciences, Medical University of Bialystok, Bialystok, Poland; 3Department of Histology and Cytophysiology, Faculty of Pharmacy, Medical University of Bialystok, Bialystok, Poland
Abstract: Polyamidoamine (PAMAM) dendrimers are multi-branched, three-dimensional polymers with unique architecture, which makes these molecules attractive for medical and pharmaceutical applications. Using PAMAM as drug carriers for topical delivery might be beneficial as they only produce a transient effect without skin irritation. To evaluate the dermal toxicity of cationic PAMAM dendrimers generation 2 and generation 3, skin irritation studies were performed in vivo in the rat skin model. After 10 days topical application of various concentrations of PAMAM-NH2 (0.3 mg/mL, 3 mg/mL, 6 mg/mL, 30 mg/mL, 300 mg/mL), skin irritation was evaluated by visual, histopathological, and immunohistochemical examination. Microscopic assessment after hematoxylin-eosin staining revealed significant morphological changes of epidermal cells after application of PAMAM-NH2 at a concentration of ≥6 mg/mL.
Morphological alterations of epidermal cells included cytoplasmic vacuolization of keratinocytes in the basal and spinous layers. Cytomorphological changes in keratinocytes, overall picture of the epidermis, and histopathological changes in the dermis were dose dependent. Detected alterations concerned hyperplasia of connective tissue fibers and leukocyte infiltration. Visible granulocyte infiltration in the upper dermis and sockets formed by necrotic, cornified cells in the hyperplastic foci of epithelium were also noted. Immunohistochemical analyses revealed that increased nuclear immunoreactivity to PCNA correlated with the concentration of PAMAM-NH2, but no significant differences in the cell proliferation activity in skin treated with PAMAM-NH2 generation 2 or generation 3 were observed. Significantly higher expression of PCNA extended throughout the skin layers might suggest abnormal cell proliferation, which, as a consequence, might even lead to neoplastic changes.
Keywords: cationic PAMAM dendrimers polymers, topical delivery, nanomaterials, in vivo toxicity, skin irritation test
Dendrimers are well-defined, highly branched macromolecules with precisely controlled chemical structure and low polydispersity. They provide a number of opportunities for design of novel drug carriers, gene delivery systems, and imaging agents.1–3 Dendrimers have been found to be suitable carriers for a variety of drugs including anticancer, antiviral, antifungal or antibacterial, with capacity to improve their bioavailability.4–8 Among existing dendrimers, polyamidoamine (PAMAM) are the most intensively investigated. They consist of ethylenediamine nucleus and branches based on methyl acrylate and ethylenediamine. Half generations of PAMAM possess carboxyl surface groups, while complete full generations have amine or hydroxyl groups. The surface groups are responsible for their high solubility and reactivity, and internal cavities can be used in encapsulation of small molecules. PAMAM dendrimers have demonstrated potential use as vehicles in several routes of administration, including oral, ocular, parenteral, and transdermal.1,9,10
It was shown that PAMAM dendrimers enhanced transdermal delivery of many drugs, including indomethacin,11 ketoprofen, diflunisal,12 8-methoxypsoralen,13,14 and 5-fluorouracil.15 The skin penetration of cationic dendrimers increased with the increase in treatment time and was inversely related to the dendrimer molecular weight.16 Interestingly, the improved penetration caused by neutral or anionic dendrimers was significantly lower. The higher skin penetration of cationic dendrimers is probably due to their binding to the negatively charged skin, interacting with the intercellular lipids,15,17 changing the architecture of the lipid bilayer18 or even inducing holes formation in the cell membranes.19 Membrane disruption by inducing formation of nanoholes or causing membrane erosion as a consequence might cause leakage of cytosolic enzymes and cell lysis.19–21 The possible clinical use of dendrimers must be preceded by extensive in vivo toxicity studies. Before Vivagel® (SPL7013) – the first product based on dendrimers (containing modified polylysine dendrimers) was introduced clinically, it was evaluated in various animal models: mice, guinea pigs, and macaques.22
Using dendrimers as drug carriers for topical delivery might be beneficial as they only produce a transient effect without skin irritation. Since, to our knowledge, there are no studies devoted to evaluation of cationic dendrimers toxicity after topical application, the goal of this work was to assess the dermal toxicity of PAMAM-NH2 dendrimers in vivo in the rat skin model. As the lower generations of cationic dendrimers showed greater penetration enhancement than the higher ones,15,17,23 PAMAM-NH2 generation 2 (G2) and generation 3 (G3) (Figure 1) were applied in this study. Skin irritation was assessed after 10 days topical application of various concentrations of PAMAM (0.3 mg/mL, 3 mg/mL, 6 mg/mL, 30 mg/mL, 300 mg/mL) by visual, histopathological, and immunohistochemical examination. Dissected skin samples were stained by hematoxylin-eosin (H and E) method and viewed using a light microscope for any pathological changes. Since PCNA immunostaining is widely used for detecting proliferating cells in tissue sections, especially of neoplastic lesions, the distribution of PCNA immunoreactivity (PCNA-IR) cells in the skin of rats treated with various concentrations of PAMAM-NH2 dendrimers was determined. The morphometric features of PCNA-IR nuclei, intensity of immunohistochemical reaction, and thickness of the epidermis were also evaluated.
Figure 1 Chemical structure of polyamidoamine-NH2 dendrimer generation 2 (A) and generation 3 (B).
Materials and methods
PAMAM dendrimers G2 and G3 with amine surface groups were provided by Sigma-Aldrich Co. (St Louis, MO, USA), as were most other chemicals used. To prepare water solutions of PAMAM, methanol was evaporated from purchased solutions by using Centrivap Concentrator FreeZone6 (Labconco, Kansas City, MO, USA). Reagents for routine histological H and E staining, a specific monoclonal mouse anti-PCNA clone PC10 M 0879, target retrieval solution S 1699, antibody diluent S 0809, and wash buffer S 3006 were obtained from Dako Denmark A/S (Glostrup, Denmark).
Male Wistar rats, weighing 150–200 g were fed a standard diet and housed in plastic cages (50/40/20 cm), one animal per cage, in an air-conditioned and temperature-controlled (21°C±2°C) room with a 12 hours light/dark cycle. Food and water were freely available. All experiments were carried out in a quiet, diffusely lit room.24 The in vivo experimental protocol was approved by the Ethics Commission of the Medical University of Białystok, Poland. On the day prior to the experiment, the animals were anesthetized with pentobarbital 40 mg/kg body weight (bw) and the hair on the dorsal side of the rats (area 4×2 cm) was carefully removed with an electric hair clipper in the direction of tail to head without damaging the skin.
The rats were divided into XII groups (n=6). Group I served as control, without any treatment; group II was administrated 0.8% aqueous solution of formalin as a standard irritant; groups III–XII were treated with 100 μL of water solutions of various concentrations of PAMAM-NH2 dendrimers G2 or G3 (0.3 mg/mL, 3 mg/mL, 6 mg/mL, 30 mg/mL, 300 mg/mL), which corresponded to 0.17, 1.67, 3.33, 16.67, and 166.67 mg/kg bw. Tested solutions were applied to the exposed skin and spread over the entire area, once a day during a 10-day period. Finally, the application sites were evaluated visually always by the same investigator and graded according to a standard visual scoring scale: 0 – no erythema, 1 – slight erythema (barely perceptible-light pink), 2 – moderate erythema (dark pink), 3 – moderate to severe erythema (light red), 4 – severe erythema (extreme redness).25 Then rats were sacrificed by decapitation under pentobarbital anesthesia (80 mg/kg bw) and dorsal skin samples from treated and untreated (control) areas were taken for histological and immunohistochemical studies. The Kruskal–Wallis analysis was used to check whether control groups were equal among themselves and to test any differences among all groups (control and experimental).
The skin samples were fixed in 4% buffered formaldehyde and routinely embedded in paraffin. Sections, 4 μm thick, were cut using rotary microtome, Leica 2025 (Leica Microsystems, Wetzlar, Germany) and stained by H and E and by Azan method for general histological examination. Tissue sections were viewed by one pathologist using a light microscope, Olympus BX41 (Olympus Corporation, Tokyo, Japan) interfaced with an image analysis system. The images were captured using a DP12 camera (Olympus Corporation).
Evaluation of cell proliferation by PCNA staining
The paraffin blocks were cut into 4 μm sections, mounted onto Superfrost Plus slides (Menzel Gläser, Braunschweig, Germany) and dried overnight at 37°C followed by 1 hour at 60°C. An immunohistochemical reactions to find PCNA was performed on paraffin skin sections of the animals. In these studies a specific monoclonal mouse anti-PCNA clone PC10 was used (M 0879; Dako Denmark A/S). The EnVision method according to Herman and Elfont was applied.26 Control reactions were simultaneously performed. In the negative control, the specific antibody was omitted in the staining procedure and control reaction performed gave negative results. Positive control was done for specific tissue recommended by producer – for PCNA it is human colon.
Immunostaining was performed by the following protocol: paraffin-embedded sections were deparaffnized and hydrated in pure alcohol. After washing with distilled water, sections were pretreated with antigen retrieval in a pressure chamber heating for 1 minute at 21 psi (1 psi equates to 6.895 kPa, the conversion factor provided by the United Kingdom National Physical Laboratory) at 125°C using target retrieval solution S 1699. After being cooled at room temperature, sections were incubated with peroxidase blocking reagent for 10 minutes to block endogenous peroxidase activity. Primary antibody was diluted 1:4,000 using the antibody diluent S 0809. The sections were incubated overnight at 4°C in a humidified chamber with the diluted antibody, followed by incubation with labeled polymer per 1 hour (EnVision System HRP Mouse Kit K4007; Dako Denmark A/S). Appropriate washing with wash buffer S 3006 was performed in-between each step. Then sections were incubated in liquid 3,3′-diaminobenzidine (+) chromogen, controlled under microscope. Finally the sections were counterstained in Vector QS hematoxylin mounted and evaluated under light microscope. The nature of staining and the distribution of PCNA-IR were determined. A cell was scored as positive when there was distinct brown granular staining of the nucleus regardless of its intensity.
Quantitative analysis of PCNA staining and imaging
The analysis of the preparations and their photographic documentation were performed using an Olympus BX41 light microscope (Olympus Corporation) equipped with Olympus DP12-2 camera (Olympus Corporation). Images from five randomly selected microscopic fields (each field 0.785 mm2), at a magnification of 200× were morphometrically evaluated by using image analysis software (NIS-Elements Advanced Research Nikon software, Nikon Instruments, Melville, NY, USA).
The number of PCNA-IR cells was counted in each analyzed image and presented as median per visual field (0.785 mm2). Morphological characteristics of PCNA-IR nuclei, (diameter, area), intensity of immunohistochemical reaction, and thickness of the epidermis were also evaluated. Intensity of immunohistochemical reaction was measured by using 0 to 256 gray scale level, where completely black pixel had a value of 0, and completely white or bright one possessed a value of 256. The gray scale intensity and PCNA expression have inverse relation.
Quantitative variables were expressed as the median with 25%–75% quartile range. A statistical analysis was performed using nonparametric technique, the Kruskal–Wallis with Dunn’s post hoc test with the Statistica 10.0 software (StatSoft, Kraków, Poland). Differences between groups were considered to be significant at P<0.05.
Results and discussion
Despite PAMAM dendrimers being promising drug delivery systems and their potential commercial applications having received considerable attention, the majority of studies performed to date focused on dendrimer toxicity evaluated in vitro. It was shown that PAMAM dendrimers demonstrated generation, surface charge and concentration dependent cytotoxicity.27–29 Assays in vitro provide cell type specific information, but do not accurately reflect dendrimers’ in vivo behavior. Limited studies have been performed to investigate dendrimer toxicity in vivo – there are only few studies concerning toxicity of PAMAM dendrimers after oral or parenteral administration.21 It was found that lower generations of PAMAM administered parenterally did not cause behavioral changes or weight loss, but for higher generations, incidents of mice death were noted. Roberts et al studied toxicity of PAMAM G3, G5, and G7 after intraperitoneal administration in Swiss-Webster mice at doses of 2.6, 10.0, and 45.0 mg/kg bw. These studies suggested that cationic dendrimers (G <7) even at high doses did not cause adverse effects.30 However, Heiden et al found that cationic PAMAM dendrimers G4 were toxic to zebrafish embryos, and the toxicity was dose and exposure duration dependent. Exposure to ≥20 μM (~0.283 mg/mL) G4 dendrimer caused 100% mortality by 24 hours post fertilization. Otherwise, in the same study anionic PAMAM dendrimers G3.5 were not toxic and reveled no signs of embryo development impairment.31 Malik et al found that 95 mg/kg bw daily doses of anionic PAMAM dendrimers (G3.5, carboxylic acid termini) administered intraperitoneally led to no mortalities and no weight change in B16F10 tumor bearing mice.32 Chauhan et al examined toxicity profile of PAMAM-NH2 and PAMAM-OH dendrimers G4 (4.75–19.0 mg/kg bw) via the intraperitoneal route for 15 days in Swiss albino mice and observed no significant effect on feed intake, body and organ weights, lipid and protein metabolism, hematological parameters, and histopathology.33 Generally, it was shown that the rank order of PAMAM toxicity is hydroxyl-terminated<carboxyl-terminated<amine-terminated dendrimers.1,29,34
Although several reports have studied PAMAM as potential skin penetration enhancers and nanocarriers for transdermal delivery,11–16,35 the toxicity of PAMAM after topical administration is largely unknown. Therefore, in this study to evaluate dermal toxicity of PAMAM-NH2 G2 and G3 after topical administration, skin irritation test in the rat skin model was performed. Rodents’ skin model (mice, rats, guinea pigs) is commonly used for irritation and permeability studies in vivo.36–38 Among rodents, rat skin is considered the most structurally similar to human tissue. However, rat skin is more permeable and more sensitive than human skin because it is significantly thinner – it possesses lower thickness of stratum corneum and epidermis.38
The skin irritation test was carried out after 10 days topical application of PAMAM by both visual observation (Figure 2A–G) and histopathological examination (Figure 3A–G). It was shown that PAMAM-NH2 G2 and G3 were well tolerated at concentrations up to 3 mg/mL. After 10 days administration, there were no signs of erythema (Figure 2C). Slight erythema in case of PAMAM-NH2 G2 at a concentration of 6 mg/mL was noted (Figure 2D). Moderate erythema (Figure 2E) and severe erythema (Figure 2F) of skin was observed in rats treated with significantly higher (30 mg/mL and 300 mg/mL, respectively) concentrations of PAMAM-NH2 G2 and 300 mg/mL PAMAM-NH2 G3 (Figure 2G).
Microscopic evaluation of the skin sections stained with H and E revealed significant morphological changes of epidermal cells after 10 days application of PAMAM-NH2 G2 at a concentration of 6 mg/mL. Morphological changes of epidermal cells included cytoplasmic vacuolization of keratinocytes in the basal and spinous layers (Figure 3D). It was also demonstrated that cytomorphological changes in keratinocytes, overall picture of the epidermis and histopathological changes in the dermis were dose dependent. Moreover, noticeable histopathological changes in the dermis after application of PAMAM at the concentration of 30 mg/mL (Figure 3E) and 300 mg/mL (Figure 3F and G) were observed. Detected alterations concerned hyperplasia of connective tissue fibers and leukocyte infiltration. Visible granulocyte infiltration in the upper dermis and sockets formed by necrotic, cornified cells in the hyperplastic foci of epithelium was also noted (Figure 3F).
The influence of PAMAM on the cell proliferation was evaluated by PCNA staining. PCNA is a 36 kDa molecular weight protein. It is an auxiliary protein for DNA polymerase delta that is involved in DNA replication as well as DNA repair mechanism. Its synthesis and expression is related to the proliferating state of the cell and its level of expression reflects cell proliferating activity.39,40 Immunohistochemical staining for PCNA allows the identification of cells in the different phases of the cycle. Expression of PCNA increases in late G1, is maximally expressed in the S phase, and decreases in G2–M phase of the cell cycle.40,41 This makes it a useful marker for proliferated cells. It is present to some degree in normal cells, while in malignancies the increase in PCNA is probably related to uncontrolled DNA synthesis and disturbed cell cycle.41,42
Immunohistochemical analyses of skin treated with various concentrations of PAMAM-NH2 G2 and G3 (0.3 mg/mL, 3 mg/mL, 6 mg/mL, 30 mg/mL, 300 mg/mL) (Figure 4A–H) revealed that increased nuclear immunoreactivity to PCNA was concentration dependent, but no significant differences in the cell proliferation activity in skin treated with PAMAM G2 or G3 was observed. Increased expression of PCNA was found in the majority of basal cell layers. However, after application of higher concentrations of PAMAM, the increased number of PCNA-IR cells was observed not only in basal layer but also in the superficial layers of epidermis (Figure 4). In the control epidermis, only few PCNA-IR nuclei were found in the cells lying in the basal layer (Figure 4A). In epidermal keratinocytes of rats treated with 0.3 mg/mL PAMAM-NH2 G2 and G3, PCNA expression was similar to the control. The expression was limited only to the cells in the basal layer, while other cell layers of the epidermis showed negative staining (Figure 4C). It was noticed that the number of PCNA-IR cells in the epidermis of skin treated with 3 mg/mL PAMAM-NH2 was higher (Figure 4D). Location of keratinocytes with PCNA-IR nuclei after application of PAMAM-NH2 6 mg/mL was significantly different from control skin tissue. As it is shown in Figure 4E, PCNA was observed in almost all the cells of the lowest layer. After administration of PAMAM-NH2 at a concentration of 30 mg/mL, a substantial increase in epidermal keratinocytes hyperplasia was noted and PCNA-IR cells were not detected only in the stratum corneum (Figure 4F). In skin of rats treated with 300 mg/mL PAMAM-NH2 G2 or G3, PCNA-IR cells significantly extended throughout the epidermis (Figure 4G and H). The amount of cells demonstrated positive nuclear staining for PCNA and the intensity of reaction is presented in Figure 5. As it is demonstrated, the rise in the amount of PCNA-IR cells and the visible increase in the intensity of immunohistochemical reaction was observed in rat skin samples after application of PAMAM-NH2 dendrimers at a concentration of 3 mg/mL. Substantial growth of the intensity of the immunohistochemical reaction in case of higher concentrations (30 mg/mL and 300 mg/mL) of PAMAM-NH2 was detected. PCNA related DNA repair in response to possible mutagens is critical to maintain the cellular genomic integrity, therefore the increase in the amount of PCNA-IR cells after application of PAMAM-NH2 is probably a consequence of enhanced DNA repair processes as a reaction to DNA damage.
As nuclear size is a very important parameter, which changes in dysplasia and reflects the intensified DNA synthesis, and the abnormalities of nuclear features have been reported in various types of carcinoma,43,44 morphological characteristics of PCNA-IR nuclei were investigated. Obtained results revealed that there was no significant differences in diameter and area of nuclei after administration of PAMAM-NH2 at concentrations up to 3 mg/mL (Figure 6). The increase in the area and diameter of the nuclei was concentration dependent. Visible growth of the nuclei area and nuclei diameter was noted at a concentration of ≥6 mg/mL of PAMAM-NH2.
The influence of various concentrations of PAMAM-NH2 on the epidermal thickness was also investigated (Figure 7). Epidermal thickness was defined as the distance between the basement membrane and the apical surface of the uppermost nucleated keratinocytes (the border between the stratum granulosum and stratum corneum).45 The epidermis is a continuously renewing tissue in which homeostasis is maintained by a regulated balance between cell proliferation, cell differentiation and programmed cell death. In the normal epidermis, proliferating cells are confined to the basal layer, whereas apoptosis appears at the border of the stratum granulosum and stratum corneum.45 As assessed by the image analyzer, the epidermal thickness of control skin samples was 21.02 μm (expressed as median). After application of PAMAM-NH2 at a concentration of 6 mg/mL, only a slight rise in the epidermal thickness was observed (25.49 μm). The increase of epidermal thickness was concentration dependent and in the group of rats treated with 300 mg/mL PAMAM-NH2 epidermal thickness (94.07 μm) was over fourfold higher than in the control group (Figure 7).
Figure 7 Effect of various concentrations of PAMAM-NH2 generation 2.
Significantly higher expression of PCNA extended throughout the skin layers, epidermal hyperplasia and increasing aberrations of nuclear features after administration of higher concentrations of PAMAM-NH2 suggest disorganized cell proliferation. Abnormal cell proliferation, which results from deregulation of the cell cycle, might even lead to neoplastic changes. In conclusion, microscopic assessment after H and E staining and immunohistochemical analyses revealed that PAMAM dendrimers with positively charged surface groups are prone to exhibit significant dermal toxicity and in potent topical applications only lower concentrations of PAMAM should be considered. Obtained data can be useful to design dendrimer-based nanocarriers for drug delivery to skin.
This research was supported by Medical University of Białystok grant (143-15780 F).
The authors declare no conflicts of interest in this work.
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