info@biomedres.us   +1 (720) 414-3554
  One Westbrook Corporate Center, Suite 300, Westchester, IL 60154, USA

Biomedical Journal of Scientific & Technical Research

May, 2021, Volume 35, 4, pp 27971-27975

Research Article

Research Article

The Effect of Chitosan Capped Copper Nanoparticles on Angiogenesis in Cam Assay

Harmankaya OF1, Hamsho A2, Goztepe M1, Baghirova S1, Cirik S3, Sirin H5, Alasad M2, Sari BS1, Uckun I1, Kocer A6, Aksu E4 and Farmanli O7*

Author Affiliations

1Kırıkkale University School of Medinice, Turkey

2Bioengineering Faculty, Kırıkkale University, Turkey

3Sakarya University School of Medicine, Turkey

4Bezmialem University School of Medicine, Turkey

5Gülhane Education and Research Hospital, School of Medicine, Turkey

6Selcuk University Vocational School of Health Services, Turkey

7Department of Pathology, Marmara University School of Medicine, Turkey

Received: May 06, 2021 | Published: May 13, 2021

Corresponding author: Farmanli Orkhan, Department of Pathology, Marmara University School of Medicine, Turkey

DOI: 10.26717/BJSTR.2021.35.005755

Abstract

Objective: Angiogenesis is the growth of blood vessels from the existing vasculature that occurs during embryonic development, wound healing, and the menstruation cycle. Chitosan is a natural cationic polysaccharide and one of the natural polymers and obtained by deacetylation of α-chitin. Chitosan-based nanoparticles show anti-cancer, anti-bacterial, anti-angiogenesis, procoagulant behaviors and good biosafety. In this study, the effects of chitosan-capped copper nanoparticles on angiogenesis in the chick chorioallantoic membrane (CAM) model were investigated.

Methods: We applied 25 mM concentrations of CuNPs solution to CAM of 15 eggs and 15 mM concentration of CuNPs solution to CAM of 16 eggs on the 5th day. After then, we evaluated results macroscopically on the 7th day.

Result: In our study, we observed that CuNPs solutions caused a significant increase in angiogenesis when compared with the control group. There was a greater increase in CAM vascular area angiogenesis of the 15mM solution group compared to the 25mM solution group.

Conclusion: The study of Ribeiro and colleagues with insulin-containing chitosan nanoparticles and our study with chitosan-coated copper nanoparticles stimulated angiogenesis. Although the study of Dragostin et al. shows that chitosan nanoparticles have an anti-angiogenic effect. We assumed that this effect may be due to copper nanoparticles as a result of our literature review.

Keywords: Angiogenesis; Chorioallantoic Membrane; Cancer; Copper Nanoparticles; Chitosan

Introduction

Angiogenesis is the growth of blood vessels from the existing vasculature [1] that occurs during embryonic development, wound healing, and the menstruation cycle. Moreover, unregulated angiogenesis (upregulation or downregulation) is seen in pathological conditions, such as psoriasis, diabetic retinopathy, and cancer [2]. Chitosan is a natural cationic polysaccharide and one of the natural polymers and obtained by deacetylation of α-chitin [3,4]. It has been included in studies that chitosan molecule is an effective transportation tool for reaching the related target with the pharmaceutical properties of various drugs [5]. Chitosan-based nanoparticles also have major effects such as anti-cancer, antibacterial, anti-angiogenesis. Moreover, it was also demonstrated that chitosan nanoparticles suppress lipopolysaccharide-induced inflammatory cascade, which is prominent in Crohn’s disease and ulcerative colitis [6]. It is known in the literature that chitosan has a procoagulant effect. Nanotoxicity study of chitosan nanoparticles was done in animal models. As a result of these studies, chitosan nanoparticles showed good biosafety [7].

Copper enters the human body through water and food, is mainly carried by plasmic proteins such as ceruloplasmin albumin, and its metabolism is in the co-factor structure of many enzymes [8]. They possess a great application in different fields such as antimicrobial activity, antifungal activity, sensors, catalysts, cytotoxicity “anticancer” activity, antioxidant activity [9]. The mesodermal layers of the allantoic and chorion fuse to form the chorioallantoic membrane (CAM) throughout avian development. CAM is an effective model to determine the behavior of normal and pathologic tissues (as cultured cells or malignant tumors). Using of various drugs, antibodies or biomaterials which placed on its surface allows us to observe angiogenesis [10]. CAM assay is preferred model by virtue of some advantages including, high embryo survival rate, easy methodology, sterility is not required, low cost, reproducibility, reliability [11]. In this study, the effects of chitosan capped copper nanoparticles on angiogenesis in chick chorioallantoic membrane (CAM) model were investigated.

Material and Methods

Material

All chemicals were analytical grade and used as purchased without further purification. Chitosan (75-85% deacetylated) the medium molecular weight chitosan is 190-310 kDa, Acetic acid (99.8-100.5%, MW=60.05 g/mol), Amonia (25%) were purchased from Iceland, SIGMA-ALDRICH Co., Ltd, Copper (II) nitrate trihydrate Cu(NO3)2*3H2O (99.0%, MW=241.60 g/mol), Carbon disulfide CS2 (99.5%, MW=76.14) were purchased Germany MERCK Co., Ltd, Sodium borohydride (96%, MW=25 g/mol) was purchased from Switzerland, FLUKA CHMIKA Co., Ltd. All solutions were prepared using double distilled water.

Synthesis of Dithiocarbamate Chitosan (DTCCS)

DTCCS were prepared with minor revision according to the method defined by Muzzarelli et al. [12], A mixture of 4g of chitosan and 0.025 mol of ammonia was stirred in ethanol 95% (v / v) at room temperature for half an hour. A solution of carbon disulfide CS2 (2 mL) was then added slowly dropwise to the solution. After stirring about 2 hours, the resulting mixture was filtered under vacuum with a filter paper and the remnant was washed by 100% of ethanol. After washed the polymer dried at 60°C. Finally, DTCCS was obtained.

Synthesis of DTCCS Capped Copper Nanoparticles

The synthesis of copper nanoparticle was done by alteration of the procedure used by Dang et al. [13], Firstly, 0.1 gr of dithiocarbamate chitosan DTCCS was dissolved in 100 ml of %1 acetic acid, then the polymer solution was added dropwise to the solution of 0.105 gr copper nitrate (Cu (NO3)2.3H2O) in 10 ml distilled water, while the color of copper solution changed from blue to light blue color. After stirring at 10,000 rpm by a high-speed homogenizer for 15 minutes the PH of the solution was changed from PH=3 to PH=6 by 1M of NaOH solution, after adding NaOH the solation color changed to be dark blue. After stirring for about 30 minutes by high-speed homogenizer 10 ml of NaBH4 was added to give a rapid brown coloration which turned to dark red after about 10 minutes of mixing. The solution was stirred for an additional 30 minutes to complete the reaction. after boiling the solution the copper nanoparticles were precipitated by centrifugation at 5,000 rpm for 15 minutes. The particles were washed repeatedly to ensure purity. Finally, the Cu-NPs were dried at 40 °C.

Fertilized Chicken Egg Preparation

For the experiment, we put 36 fertilized chicken eggs in an incubator at 37°C and 85-90% relative humidity. We kept it in the incubator for 5 days. Then, on the 5th day, we pierced the eggshell in the place corresponding to the CAM of the chicken eggs. We applied the CuNPs solution on the CAM and covered the hole of each egg with paraffin tape. Then we put the eggs back in the incubator. We kept it in the incubator at suitable temperature and humidity for 48 hours after the application. At the end of the 48th hour, we evaluated the vascular development macroscopically on the CAM and photographed with a stereomicroscope attached to a digital camera.

Application of the Solution to Fertilized Chicken Eggs

On the 5th day, we pierced the eggshell in the place corresponding to the CAM of the chicken eggs. Before the application, we photographed the CAMs of the eggs with a stereomicroscope connected to a digital camera. We applied 15 mM and 25 mM of CuNPs solution to each CAM surface. After the application, we closed the holes of each egg with paraffin tape. We grouped and numbered eggs with 15mM and 25mM CuNPs solution applied [14]. Then we kept it in the incubator for 48 hours at suitable temperature and humidity. On the 7th day, we removed the paraffin tape on the CAM. All eggs were observed macroscopically and photographed with a stereomicroscope connected to the digital camera. Using the Knighton et al. score, the vascularization increases in the photographs taken on the 5th and 7th days were scored by 3 observers [15].

Result

On the 5th day we pierced the eggshell. We used 36 eggs for this study. We established 3 eggs died before the application of CuNPs solutions. Two of 33 eggs were used as controls. We applied 20mL volume CuNP solution in different concentrations to the CAM of the remaining 31 eggs. We applied 25 mM concentrations of CuNPs solution to CAM of 15 eggs and 15 mM concentration of CuNPs solution to CAM of 16 eggs on the 5th day.

On the 7th day, CAMs of eggs were evaluated macroscopically by 3 researchers. We rated effects CuNPs solution on CAM vessel growth and angiogenesis (Figures 1-3). The treatment of CAM with 25 mM CuNPs solutions caused a significant development in CAM vascular area of 7 eggs. And the treatment of CAM with 15mM CuNPs solutions cause a significant development in CAM vascular area of 10 eggs. CuNPs solutions caused a significant increase in angiogenesis when compared with the control group. There was a marked increase in angiogenesis in both groups. But there was a greater increase in CAM vascular area angiogenesis of the 15mM solution group compared to the 25mM solution group. We have shown the macroscopic results of vascular development of CAM of different concentrations of CuNP solution on CAM in Table 1.

Table 1: Macroscopic evaluation of the effect of CuNPs treatment on CAM.

Figure 1: There is no any injection to A and B. As seen macroscopically there is no significant changes of angiogenesis status.

Figure 2: A. Before injection of CuNPs B. After injection of CuNPs. As seen macroscopically angiogenesis increased (+2) after injection.

Figure 3: A. Before injection of CuNPs B. After injection of CuNPs. As seen macroscopically angiogenesis increased (+1) after injection.

Discussion

Angiogenesis is the process of generating new blood vessels and have essential roles in many pathological conditions [16]. Because of high sensitivity, being cheap and easy CAM model of chick embrios is mostly used as an in-vivo working model for angiogenesis [17]. Copper is a essential microelement required by animals and humans. Although the content of Cu in the human body is very low but it plays an important and multifunctional role as a cofactor of many enzymes [18]. Cu has essential role in angiogenesis as a stimulator of angiogenesis, vasculogenesis and endothelial cell migration [19]. Cu has been shown to stimulate angiogenesis in chick embryo chorioallantoic membrane (CAM) models [20]. Chitosan is the product of the complete or partial deacetylation of chitin. Chitosan is a widely used excipient for topical or oral drug administration. It is also now considered as a useful material for drug and gene delivery systems for parenteral administration [21]. Chitosan has been shown to inhibit angiogenesis in chick embryo chorioallantoic membrane (CAM) models [22].

Up to now, no study has been observed about angiogenic effect of Chitosan capped Copper nanoparticles except Mroczek- Sosnowska et al. manuscript on chick chorioallantoic membrane assay in literature. Natalia Mroczek-Sosnowska et al. investigated the effect of copper nanoparticles on angiogenesis in CAM assay at the systemic and molecular level. As a result of the study, they proved that copper nanoparticles increase angiogenesis [18]. In a study by Yannan Li et al., the effect of copper on angiogenesis was examined using hydrogel scaffold. As a result of the study, they established that copper increases angiogenesis by increasing HIF- 1α / VEGF expression [23]. As a result of our literature review about chitosan, we encountered a manuscript by Dragostin et al. They demonstrated the anti-angiogenic effect of chitosan nanoparticles in CAM assay [22]. In another study, Ribeiro and colleagues have shown that insulin-containing chitosan nanoparticles stimulate angiogenesis [24]. We thought this effect could be due to insulin. Similarly, in our study, chitosan coated copper nanoparticles stimulated angiogenesis. We assumed that this effect may be due to copper nanoparticle as a result of our literature review.

Consequently, Chitosan and copper nanoparticles are biomaterials in which experimental research are carried out in many areas such as cancer treatments, drug administrations, scaffolds. Therefore, it is essential to know the mechanism of action of these molecules. In our study, we also focused on the effects on angiogenesis which has an important role in many pathology processes. As a result of the study, we established that chitosan coated copper nanoparticles stimulate angiogenesis. Further studies are required.

Conflict of Interest

None.

References

Research Article

The Effect of Chitosan Capped Copper Nanoparticles on Angiogenesis in Cam Assay

Harmankaya OF1, Hamsho A2, Goztepe M1, Baghirova S1, Cirik S3, Sirin H5, Alasad M2, Sari BS1, Uckun I1, Kocer A6, Aksu E4 and Farmanli O7*

Author Affiliations

1Kırıkkale University School of Medinice, Turkey

2Bioengineering Faculty, Kırıkkale University, Turkey

3Sakarya University School of Medicine, Turkey

4Bezmialem University School of Medicine, Turkey

5Gülhane Education and Research Hospital, School of Medicine, Turkey

6Selcuk University Vocational School of Health Services, Turkey

7Department of Pathology, Marmara University School of Medicine, Turkey

Received: May 06, 2021 | Published: May 13, 2021

Corresponding author: Farmanli Orkhan, Department of Pathology, Marmara University School of Medicine, Turkey

DOI: 10.26717/BJSTR.2021.35.005755

Abstract

Objective: Angiogenesis is the growth of blood vessels from the existing vasculature that occurs during embryonic development, wound healing, and the menstruation cycle. Chitosan is a natural cationic polysaccharide and one of the natural polymers and obtained by deacetylation of α-chitin. Chitosan-based nanoparticles show anti-cancer, anti-bacterial, anti-angiogenesis, procoagulant behaviors and good biosafety. In this study, the effects of chitosan-capped copper nanoparticles on angiogenesis in the chick chorioallantoic membrane (CAM) model were investigated.

Methods: We applied 25 mM concentrations of CuNPs solution to CAM of 15 eggs and 15 mM concentration of CuNPs solution to CAM of 16 eggs on the 5th day. After then, we evaluated results macroscopically on the 7th day.

Result: In our study, we observed that CuNPs solutions caused a significant increase in angiogenesis when compared with the control group. There was a greater increase in CAM vascular area angiogenesis of the 15mM solution group compared to the 25mM solution group.

Conclusion: The study of Ribeiro and colleagues with insulin-containing chitosan nanoparticles and our study with chitosan-coated copper nanoparticles stimulated angiogenesis. Although the study of Dragostin et al. shows that chitosan nanoparticles have an anti-angiogenic effect. We assumed that this effect may be due to copper nanoparticles as a result of our literature review.

Keywords: Angiogenesis; Chorioallantoic Membrane; Cancer; Copper Nanoparticles; Chitosan