Trends in
Biomaterials & Artificial Organs
An International Journal Published by the 
Society for Biomaterials and Artificial Organs India

ISSN 0971-1198 (print)
Volume 22, Number 3, January-April 2009 

Full text can be accessed by clicking on the pdf link.

The journal has now initiated online manuscript submission and peer-review management system in technical collaboration with www.criticalmath.com . Authors can now submit their manuscripts at http://tbao.criticalmath.com .

Editorial
Chandra P Sharma: A 60th Birthday Celebration


p 125-137

Antibacterial Activity of Chitosan Chemically Modified with New Technique

M.S. Mohy Eldin1*, E.A. Soliman1, A.I. Hashem2, T.M. Tamer1

1Polymer Materials Research Department,
Advanced Technologies and New Materials Research Institute (ATNMRI),
Mubarak City for Scientific Research and Technology Applications (MUCSAT),
New Borg El-Arab City 21934, Alexandria, Egypt.
2Organic Chemistry Department,
Faculty of Science, Ain-Shams University,
Cairo, Egypt.

*
Corresponding author: mohyeldinmohamed@yahoo.com

Received 01 May 2008; Accepted 25 November 2008; published online 23 December 2008

The antibacterial activity of chitosan was chemically modified by introducing further amino groups to the back bone of chitin using parabenzoquinone (pBQ) as activation agent and ethylene di amine (EDA) as amino group source. The aminated chitin was further deacetylated to obtain finally chemically modified chitosan with higher content of amine groups. Factors affecting both activation process, and amination process amine grafting, have been studied through following its effect on the amount of introduced amine groups. The success of grafting process has been confirmed using FT-IR and TGA analysis. The antibacterial activity of the modified chitosan was tested on four different bacterial strains; two gram negative (Escherichia coli, pseudomonas aeruginosa), and two gram positive (Bacillus cereus, Staphylococcus aureus). It was found that the antibacterial activity of the modified chitosan is better than the native one, and increases by increasing the amount of introduced amine group (degree of the grafting), the degree of deacetylation. Lowering the molecular weight was found of negative effect. On the other hand, The Cytotoxicity activity test using Caco 2 cell line shows a safety result. As chitosan, modified chitosan show potential bactericidal activity along all strain examined spatially on the gram negative bacteria (Escherichia coli, pseudomonas aeruginosa). Finally, the modified chitosan shows higher solubility, almost double, at pH range from 5 to 6 comparing to chitosan it self. 

© Society for Biomaterials and Artificial Organs (India), 20080501-18.


p 138-143

Comparative Study of the Behaviour of a Novel Injectable Bioceramic in Sheep Vertebrae

Leif Hermansson1, Urban Höglund2, Erik Olaisson1, Peter Thomsen3, Håkan Engqvist4
1Doxa AB, Sweden, 2Visionar AB, Sweden, 3Sahlgrenska Academy, Gothenburg University, Sweden
4Engineering Sciences, The Angstrom Laboratory, Uppsala University

Received 04 May 2008; Accepted 25 November 2008; published online 23 December 2008

Biomaterials used for vertebral compression fractures (VCFs) have previously mainly been based on conventional bone cement, polymethyl methacrylate (PMMA). New alternative materials based on bio-ceramics, e.g. calcium aluminate cements (CAC), are under development. In this in vivo study the biocompatibility and degree of integration/healing was compared between bone and three different cements used for VCFs; Xeraspine™ (a calcium aluminate-based cement), Cortoss™ (a bisphenol-a-glycidyl dimethacrylate based material) and conventional bone cement, Vertebroplastic™ (PMMA) in sheep vertebrae. In addition to an attempt to localize histologically depositions of aluminium aluminium in serum and in selected organs was quantified. Also, histopathological evaluation was conducted to determine the immunological response in the vertebrae caused by the different materials. It was found that Xeraspine was well accepted by the sheep vertebrae and the results were comparable to those of the other cements studied. 

© Society for Biomaterials and Artificial Organs (India), 20080504-19.


p 144-157

How is the Surface Treatments Influence on the Roughness of Biocompatibility?

Mohammad Mohsin Hossain*, Wei Gao

Department of Chemical & Materials Engineering, 
The University of Auckland, Private Bag 92014,
Auckland City, New Zealand.
*corresponding author,
mhos041@ec.auckland.ac.nz

Received 17 May 2008; Accepted 25 November 2008; published online 23 December 2008

It is well known that the extensive uses of biomaterial for biomedical implantation depend on biocompatibility. In order to improve biocompatibility of titanium alloys several factors are needed to be studied. These factors include surface roughness, surface coating materials, surface oxide film and apatite-forming-ability. There are inadequate results existed in literatures on how bioactive material surface to be processed to become a secure surface oxide film on the substrates. There are also imperfect information about the bonding strength between the surface oxide film and bioactive material. So, the firm of surface oxide film by physico-chemical process is the key premise for future development of bioactive material. The rationale of literature surveys to find out the most convenient techniques for measuring surface roughness, modifying surface oxide film and effective applications in biomedical implantation. 

© Society for Biomaterials and Artificial Organs (India), 20080517-20.


p 158-168

 

Chitosan Modified Membranes for Wound Dressing Applications: Preparations, Characterization and Bio-Evaluation

M.S. Mohy Eldin1*, E.A. Soliman1, A.I. Hashem2, T.M. Tamer1

1Polymer Materials Research Department 
Advanced Technologies and New Materials Research Institute (ATNMRI), 
Mubarak City for Scientific Research and Technology Applications (MUCSAT), 
New Borg El-Arab City 21934, Alexandria, Egypt.
2 Organic Chemistry Department, faculty of science Ain-Shams University

*
Corresponding author, mohyeldinmohamed@yahoo.com

Received 19 May 2008; Accepted 25 November 2008; published online 23 December 2008

Modified chitosan membranes for wound dressing application has been prepared, characterized and evaluated. New chemical route has been used to modify antibacterial activity of chitosan through grafting of extra amine groups in addition to the original ones. This process has been verified with FT-IR analysis and solubility test.. The prepared membranes from modified chitosan were characterized from physicochemical point of view. Properties like water uptake, tensile strength, elongation, water vapor permeability and surface roughness have been monitored. Evaluation of the membranes as wound dressing has been done through investigation of its antibacterial activity against different microorganisms, gram negative and gram positive bacteria, cytotoxicity, biodegradability and Haemocompatability. The modified chitosan membranes show high profile as a wound dressing biomaterial.

© Society for Biomaterials and Artificial Organs (India), 20080519-21.


p 169-178

Development and Characterization of Polymer Ceramic Composites for Orthopedic Applications

J. Kamaraj, E. Swaminathan, S. Dharmalingam *

Department of Chemistry, Anna University Chennai, Chennai-600025, India
* Corresponding author,
sangeetha@annauniv.edu

Received 01 July 2008; Accepted 25 November 2008; published online 23 December 2008

In the present work, synthetic composites were prepared using Polyether ether ketone (PEEK) and Poly styrene (ethylene-butylene) polystyrene (PSEBS) as polymer matrices and Hydroxyapatite as the ceramic. In order to have chemical interactions possible with –OH group of Hydroxyapatite, the polymers were sulphonated. By doing so, the drawback of Hydroxyapatite, i.e., its migration from the site of implant in the body can be avoided. Thus a better interface of Hydroxyapatite with the polymer matrix can be expected. In order to study the effect of biocompatibility of HAP in sulphonated PEEK and PSEBS, a series of two sets of composites (each having 5 different proportions) were prepared. Then, the water swelling studies, biocompatibility tests were performed. Biocompatibility tests include clot formation test, % Haemolysis and protein adsorption test. Then the prepared composites were characterized by FT-IR, XRD and TGA.

© Society for Biomaterials and Artificial Organs (India), 20080701-21.


p 179-201

Electrospinning of Chitin and Chitosan Nanofibres

C. K. S. Pillai and Chandra P. Sharma*

Division of Biosurface Technology, Biomedical Technology Wing,
Sree Chitra Thirunal Institute for Medical Sciences & Technology,
Poojappura, Thiruvananthapuram 695 012 INDIA
* Corresponding author sharmacp@sctimst.ac.in 

Received 5 February 2009; Accepted 25 February 2009; published online 17 March 2009

The electrospinning technique is a versatile method to spin polymers into continuous fibers with diameters ranging from a few micrometers to a few nanometers. Electrospinning creates seemingly endless ultra fine fibers that collect in a random pattern. These nanofibers can form non-woven textile mats, oriented fibrous bundles and even three-dimensional structured scaffolds, all with large surface areas and high porosity. It is, thus, the most extensively used fabrication method that offers vast opportunities for control of the morphology of the electrospun fibers. Due to their intrinsic features, polymeric nanofibers are attractive for biomedical and biotechnological applications such as tissue engineering, nanocomposites for dental application, controlled drug delivery, medical implants, wound dressings, biosensors and filtration. The applications of chitin and chitosan (CS) nanofibers in these areas are reviewed in this paper. Because of the inherent biodegradability, biofunctionality and biocompatibility of the biopolymer, electrospun chitin and CS fibers have special advantages whereby properties such as cytocompatibility, tissue responses etc. could be controlled in critical applications.

© Society for Biomaterials and Artificial Organs (India), 20090205-21.


p 202-210

Bioactivity Enhancement of Commercial Pure Titanium by Chemical Treatments

A Thirugnanam, TS Sampath Kumar* and Uday Chakkingal

Department of Metallurgical and Materials Engineering,
Indian Institute of Technology Madras, Chennai 600036, India
*Corresponding author: TS Sampath Kumar, tssk@iitm.ac.in 

Received 3 January 2009; Accepted 30 January 2009; published online 30 January 2009

Commercial pure titanium (cpTi) sheets were subjected to various chemical treatments to study the role of surface chemistry, morphology etc., on improving the bioactivity, the ability to form hydroxyapatite (HA) coating in simulated body fluid (SBF). Both the treated and untreated samples were characterized before and after immersing in SBF by X-ray powder diffraction, scanning electron microscopy and atomic force microscopy techniques. The combination of acid plus alkali treatment seems to nucleate more and dense HA compared to other treatments. The HA nucleates initially along the grain boundaries and then homogenously with immersion time. The overall effect of grain boundary and roughness leading to the formation of higher amount of sodium titanate gel has been proposed for the bioactivity enhancement of cpTi by the proposed surface treatment. 

© Society for Biomaterials and Artificial Organs (India), 20090103-33.


p 211-215

Method to Enhance the Encapsulation of Biologically Active Molecules in PLGA Nanoparticles

Sanju Sourabhan, K. Kaladhar, Chandra P. Sharma*

Division of Biosurface Technology, Biomedical Technology Wing
Sree Chitra Tirunal Institute for Medical Sciences & Technology
Poojappura Thiruvananthapuram 695012 INDIA
*corresponding author e-mail: sharmacp@sctimst.ac.in  (Dr. C.P. Sharma)

Received 19 January 2009; Accepted 30 January 2009; published online 30 January 2009

Biodegradable poly lactide-co-glycolide nanoparticles have been widely explored as carriers for biologically active molecules in drug delivery. Several techniques are used for the production of PLGA nanoparticles, such as those by double-emulsion technique, phase separation or spray drying. Various factors govern the drug encapsulation and release characteristics, such as the polymer characteristics, particle size etc. To improve the therapeutic efficacy, the encapsulation efficiency of drug delivery system must be optimized. In this study, a novel method was used to enhance the encapsulation of the biologically active macromolecules such as protein (albumin) and DNA. This compartmentalization strategy enhanced the encapsulation upto 98% in DNA and 93% in protein. Addition of sucrose during lyophilization also improved the stability of protein and DNA, however agglomeration was seen in case of DNA. The present study would provide a platform for producing nanoparticles with high loading and release characteristics with reference to macromolecular drugs. 

© Society for Biomaterials and Artificial Organs (India), 20090119-21.


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