SciELO - Scientific Electronic Library Online

 
vol.56 número4SYNTHESIS, CHARACTERIZATION AND ANTIHYPERTENSIVE ACTIVITY OF SOME NEW SUBSTITUTED PYRIDAZINE DERIVATIVESREGIOSELECTIVE AND HIGH-YIELDING BROMINATION OF PHENOLS AND ANILINS USING N-BROMOSACCHARIN AND AMBERLYST-15 índice de autoresíndice de assuntospesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Journal

Artigo

Indicadores

Links relacionados

Compartilhar


Journal of the Chilean Chemical Society

versão On-line ISSN 0717-9707

J. Chil. Chem. Soc. vol.56 no.4 Concepción dez. 2011

http://dx.doi.org/10.4067/S0717-97072011000400007 

J. Chil. Chem. Soc., 56, No 4 (2011), págs: 860-862

 

BIOMIMETIC CALCIUM CARBONATE IN THE CARBOXYMETHYL CHITOSAN /BOVINE SERUM ALBUMIN SYSTEM

 

CHENG-LI YAO, JIN-MIAO ZHU, AI-MING DING1*

Department of Chemistry, Hefei Normal University, Hefei, Anhui, 2 30061, China. clyao75@gmail.com


ABSTRACT

Being a biocompatible, biodegradable and bioactive material, chitosan in the form of membranes offers a great potential as a substrate in mineralization processes in vitro. In the present work, chitosan with (without) bovine serum albumin used as templates induced the formation of calcium carbonate. The unusual morphology of calcium carbonate was get from the chitosan /bovine serum albumin system. The CaCO3 crystals obtained in system were characterized by scanning electron microscopy, Fourier transform infrared spectrography and powder X-ray diffractometry. The possible formation mechanism of CaCO3 was discussed.

Keywords: Bovine Serum Albumin, carboxymethyl Chitosan, Calcium Carbonate, Biomineralization.


INTRODUCTION

Chitosan is a partially deacetylated polymer of N-acetyl glucosamine. It is essentially a natural, water-soluble, derivative of cellulose with unique properties. Chitosan is usually prepared from chitin (2 acetamido-2-deoxy β-1,4-D-glucan) and chitin has been found in a wide range of natural sources (crustaceans, fungi, insects, annelids, molluscs, coelenterata etc.) 1Specifically, it is a biocompatible, antibacterial and environmentally friendly polyelectrolyte, thus lending itself to a variety of applications2 including water treatment, chromatography, additives for cosmetics, textile treatment for antimicrobial activity3, novel fibers for textiles, photographic papers, biodegradable films4, biomedical devices, and microcapsule implants for controlled release in drug delivery5-7.

In the shell of mollusk, the formation of nacre layers is closely related to the templating effect of organics during the crystallization of calcium carbonate; therefore, investigation into the roles of different organics involved in the crystallization is crucial in understanding biomineralization 8.

Among the most current topics in this field is the adaptation of in vitro biomineralization experiments to resemble conditions in vivo more closely with two aims in mind. One aim is to gain further knowledge about basic principles of biomineralization and the second is to use this knowledge for biomimetic processing of biomaterials, with applications envisaged in bone tissue engineering especially 9. Formation of CaCO3 films on the surface of chitosan membranes has been studied by some researches 10-14.

We chose carboxymethyl chitosan and bovine serum albumin as matrices because they can be considered synthetic analogues of insoluble and soluble matrices in nacre, respectively. Moreover, the cooperative effects of carboxymethyl chitosan and bovine serum albumin yield aragonite thin films15-23. It has often been observed that the presence of bovine serum albumin induces the formation of aragonite crystals 16-17.

This paper focuses on study of the growth of CaCO3 crystals in carboxymethyl chitosan mixed bovine serum albumin system. From the experiments we expect to find carboxymethyl chitosan -bovine serum albumin how to induce the formation of calcium carbonate.

MATERIALS AND METHODS

Chitosan and Bovine Serum Albumin (BSA) were obtained from Aldrich Chemical Company Inc, acetic acid (AR), anhydrous sodium carbonate (AR) and anhydrous calcium chloride was obtained from Shanghai Chemical Reagent Company. All reagents were used without further purification.

The preparation of carboxymethyl chitosan was prepared according to the previously described methods 24. Chitosan was dissolved in 40-50% (w/w) NaOH solution, appropriate volume of isopropanol was added, and then chloroacetic acid was added slowly to the mixed solution. The pH value of reaction solution was adjusted to 7.0 with dilute aqueous HCl solution and the reaction was allowed to proceed at 60°C. The obtained mixture was precipitated with acetone, washed with anhydrous alcohol at least three times, and the product was dried in vacuum.

The carboxymethyl chitosan used as the system for the growth of CaCO3 crystal, 8g of carboxymethyl chitosan was added to 400 ml of distilled water and stirred at room temperature for 40 min. Then 400mL carboxymethyl chitosan solution was divided into four equal portions which were labeled CS(A), CS(B), CS(C), CS(D) respectively. At the same time there were 0 mg, 80 mg, 160 mg, 320 mg BSA sadded to the CS(A), CS(B), CS(C) , CS(D) respectively. After the addition of bovine serum albumin (BSA), the system was stirred slowly in order to make the solution uniform.

0.8 g of anhydrous sodium carbonate was placed at the bottom of a large beaker (250 mL), and the same amount of anhydrous calcium chloride was placed at the bottom of a small beaker (100 mL). The small beaker was placed in the large beaker. The CS(A), CS(B), CS(C), CS(D) was added to the two beakers, respectively. In the experiments carboxymethyl chitosan solution was not added to the beaker until the solution surface exceeded the inner small beaker wall by 5, 6 mm. The solution was kept at 37±0.1, °C for 7 days without stirring. When a large number of crystals present in the reaction vessel, the crystalline calcium carbonate was collected, vacuum-filtered and washed with distilled water and then with anhydrous ethanol. The crystals were dried in vacuum for 48 h and kept in a desiccator. The obtained crystalline CaCO3 was collected for the determination of SEM, FT-IR and XRD.

RESULTS AND DISCUSSION

Figure1a~d showed SEM pictures of CaCO3 particles precipitated in 2% (w/w) of carboxymethyl chitosan with different concentrations BSA. Figure1a showed there were irregular particles formed which composed of a little rhomboidal particles. With the increase of BSA concentration, cauliflower-shaped crystals formed in the system (Figure1b).When the BSA concentration was up to 1.6mg/mL, symmetric dendrite-shaped CaCO3 particles were found in the system (Figure1c). Surprisingly, when BSA=3.2mg/mL, symmetric dendrite-shaped CaCO3 particles were disappeared instead of rice ear-shaped particles (Figure1d). These results indicate that BSA had significant influence on the morphology of CaCO3 in the carboxymethyl chitosan system.


Infrared spectra of CaCO3 crystals produced in different concentration of BSA in the carboxymethyl chitosan system were shown in Figure 2. While in Figure 2a-d, simultaneous occurrence of absorption peaks at 874and 712cm-1 indicated the presence of crystalline calcite25. The slight discrepancy between experimental and published IR values could be attributed to the required grinding of a CaCO3 sample with KBr to produce pellets. There was little difference among those four curves. Figure 3 shows the XRD patterns of CaCO3 particles obtained in different concentrations of BSA in the chitosan systems. Using the reflection peaks at (104) plane for calcite, we can find that particles were all calcite.




According to our previous work 26-27, we think the carboxymethyl chitosan acts as agarose molecules in the biomineralization of calcium carbonate. Carboxymethyl chitosan molecules maybe do not directly affect the crystallization of CaCO3 which just plays a role of reaction media that control the diffusion process of ions in the media and hinder the crystal growth when the crystal size reaches the pore size of the carboxymethyl chitosan network (Figure 4).


Based on some related researches 26-28, we learn some important information. The formation of CaCO3 in the carboxymethyl chitosan system with BSA should be equalized by the interplay of two parallel phenomena: First,BSA-Ca2+ polyelectrolyte composites form in the CaCl2 solution, then the electrostatic force between the-COO- and the-NH3+ groups, and moreover, the hydrogen bond between-COOH and-OH,-NH2 groups in the network framework of carboxymethyl chitosan, will lead to the local high supersaturation with CaCO3 around the membrane when CO32- is diffused into the CaCl2 solution; Second, BSA remains as mobile polar groups in the form of BSA-Ca2+ in the system, and thus inhibits the growth of the crystals in the CaCO3 solution by its adsorption. During the formation of calcium carbonate, the nucleation and growth of the crystals may be affected by the carboxymethyl chitosan/bovine serum albumin through electrostatic matching, structural and interfacial molecular recognition. The stereo-structure of the crystal nucleus may be affected by this interfacial molecular recognition. And the activation energy of nucleation (ΔG*) may be decreased by interfacial molecular recognition. With the decrease of ΔG*, the vaterite may be more easy formed and exist under this condition. The combination of these phenomena will result in a high supersaturation with CaCO3 in the carboxymethyl chitosan framework vicinity, which causes the kinetically controlled condition for crystallization and therefore leads to the formation of cauliflower-shaped crystals.

CONCLUSION

In our investigation, an easy route nucleation model is employed in the nucleation of CaCO3 under the influence of BSA in the carboxymethyl chitosan system. The results indicated that the carboxymethyl chitosan plays a role like as agarose molecules in the biomineralization of calcium carbonate. Carboxymethyl chitosan molecules just play a role of reaction media that control the diffusion process of ions in the media and hinder the crystal growth. In the carboxymethyl chitosan system, bovine serum albumin will induce different shape calcium carbonate crystals but same crystal form. This research may provide new insights into the control of morphologies of CaCO3 and the controllable synthesis of novel inorganic materials.

ACKNOWLEDGEMENTS

The authors acknowledge the financial support provided by Natural Science Foundation of the Education Department of Anhui Province (No. KJ2011Z312) and key discipline of hefei normal University for carrying out this work.

 

REFERENCES

1. R Shepherd, S Reader ,A Falshaw, Glycoconjugate Journal, 14,535, (1997)        [ Links ]

2. Shiro Kobayashi, Toshitsugu Kiyosada, Shinichiro Shoda, Journal of the American Chemical Society, 118,13113,(1996)        [ Links ]

3. Younsook Shin, Dong Il Yoo, Kyunghye Min, Journal of Applied Polymer Science, 74,2911,(1999)        [ Links ]

4. Shigehiro Hirano, Yasuo Koishibara, Biochemical Systematics and Ecology, 19,379, (1991)        [ Links ]

5. A. D. Sezer, J. Akbuga, Journal of Microencapsulation, 16,687, (1999)        [ Links ]

6. A. Bartkowiak, D. Hunkeler, Chemistry of Materials, 11,2486,(1999)        [ Links ]

7. Takahiro Suzuki, Yasuyuki Mizushima, Tomohiro Umeda, Ryo Ohashi, Journal of Bioscience and Bioengineering, 88,194, (1999)        [ Links ]

8. L.Addadi, D. Joester, F. Nudelman, S. Weiner, Chemistry-A European Journal, 12, 981,(2006)        [ Links ]

9. A. L. Oliveira, J. F. Mano, R. L. Reis, Current Opinion in Solid State & Materials Science, 7,309, (2003)        [ Links ]

10. Linghao He, Rui Xue, Rui Song,Journal of Solid State Chemistry, 182,1082,( 2009)        [ Links ]

11. Takashi Kato, Takuo Suzuki, Takahiro Amamiya, Taku Irie, Makoto Komiyama, Supramolecular Science, 5,411, (1998)        [ Links ]

12. Sukun Zhang, K. E. Gonsalves, Materials Science and Engineering: C, 3,117, (1995)        [ Links ]

13. L. A. Gower, D. A. Tirrell, Journal of Crystal Growth, 191,153, (1998)        [ Links ]

14. Fengying Zhang, Jie Wang, Zhengchi Hou, Zhengchi Hou, Ming Yu, Leidong Xie, Materials & Design, 27,422, (2006)        [ Links ]

15. N. Hosoda, T.Kato, Chemistry of Materials, 13, 688,(2001)        [ Links ]

16. A. Sugawara, T. Kato, Chemical Communications, 6, 487,(2000)        [ Links ]

17. A. Sugawara, T.Kato, Composite Interfaces, 11, 287, (2004)        [ Links ]

18. T. Kato, Advanced Materials, 12, 1543, (2000)        [ Links ]

19. S. Zhang, K. E. Gonsalves, Langmuir, 14, 6761, (1998)        [ Links ]

20. S. Zhang, K. E. Gonsalves, Journal of Applied Polymer Science, 56, 687, (1995)        [ Links ]

21. A. Kotachi, T. Miura, H. Imai, Chemistry Letters, 32,820, (2003)        [ Links ]

22. A. Kotachi, T. Miura, H. Imai, Chemistry of Materials, 16, 3191,(2004)        [ Links ]

23. T. Iwatsubo, K.Sumaru, T.Kanamori, T. Yamaguchi, T. Sinbo, Journal of Applied Polymer Science, 91,3627,(2004)        [ Links ]

24. Yu-hua Shen, An-jian Xie, Xue-rong Yu, Gang Wu, Ling-guang Qiu, Shi-kuo Li, Xiang-yun Kong,Cheng-Xiang Han, Colloid Journal, 69,348, (2007)        [ Links ]

25. John R. Clarkson, Timothy J. Price ,Christopher J. Adams, Journal of the Chemical Society, Faraday Transactions, 88,243,(1992)        [ Links ]

26. Cheng-Li Yao, Chun-Xia Qi, Jin-Miao Zhu,Wang-Hua Xu, Journal of the Chilean Chemical Society, 55,270,(2010)        [ Links ]

27. Cheng-Li Yao, Wang-Hua Xu, Ai-Min Ding, Jin-Miao Zh, Asian Journal of Chemistry, 22, 733, (2010)        [ Links ]

28. Wang Jinn-Mei,YAO Sony-Nian,Chinese Journal of Inorganic Chemistry, 18,249, (2002)        [ Links ]

 

(Received: November 10, 2011 - Accepted: July 6, 2011)

Creative Commons License Todo o conteúdo deste periódico, exceto onde está identificado, está licenciado sob uma Licença Creative Commons