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Singh, Anil Kumar
- Biocompatibility Studies of Electron Beam Cured Pressure Sensitive Adhesive Tape for Medical Application
Abstract Views :292 |
PDF Views:103
Authors
Affiliations
1 Shriram Institute for Industrial Research, 19-University Road, Delhi 110 007, IN
2 Vinoba Bhave University, Hazaribag, Jharkhand 825 301, IN
1 Shriram Institute for Industrial Research, 19-University Road, Delhi 110 007, IN
2 Vinoba Bhave University, Hazaribag, Jharkhand 825 301, IN
Source
Current Science, Vol 110, No 6 (2016), Pagination: 1023-1030Abstract
Polyurethane (PU)-based pressure-sensitive adhesive (PSA) tapes are commonly used during surgery. Such devices made for biomedical applications must be biocompatible and biologically safe while in use in the human body as their ingredients may leach off of a device into an adjacent tissue and can harm the body during or after application. In the present study, various methods required for biocompatibility establishment, e.g. cytotoxicity, irritation and sensitization for a device, have been analysed and presented following suitable specifications. The study also emphasizes on the developmental and curing mechanism of biomedical adhesive tape by electron beam (e-beam) irradiation.References
- ISO 10993-1, Biological evaluation of medical devices-part 1, evaluation and testing in the risk management process, 2009.
- ISO 10993-2, Biological evaluation of medical devices-part 2, animal welfare requirements, 2006.
- ISO 10993-5, Biological evaluation of medical devices-part 5, tests for in vitro cytotoxicity, 2009.
- ISO 10993-10, Biological evaluation of medical devices-part 10, tests for irritation and skin sensitization, 2010.
- ISO 10993-12, Biological evaluation of medical devices-part 12, sample preparation and reference materials, 2012.
- Singh, A. K., Mehra, D. S., Niyogi, U. K., Sabharwal S. and Khandal, R. K., Polyurethane based pressure sensitive adhesives (PSAs) using e-beam irradiation for medical application. J. Polym.Material., 2011, 28(4), 525–542.
- Singh, A. K., Mehra, D. S., Niyogi, U. K., Sabharwal, S. and Khandal, R. K., Effect of tackifier and crosslinkers on electron beam curable polyurethane pressure sensitive adhesive. Radiat.Phys. Chem., 2012, 81(5), 547–552.
- Singh, A. K., Mehra, D. S., Niyogi, U. K., Sabharwal, S., Swiderska, J., Czech, Z. and Khandal, R. K., Effect of crosslinkers on adhesion properties of electron beam curable polyurethane pressure sensitive adhesive. Int. J. Adhes. Adhes., 2013, 41, 73– 79.
- Singh, A. K., Niyogi, U. K., Sabharwal, S., Kowalczyk, A., Czech, Z. and Mehra, D. S., Shrinkage studies in electron beam curable polyurethane pressure sensitive adhesive. J. Adhes. Sci. Technol., 2013, 27(14), 1511–1524.
- Singh, A. K., Mehra, D. S., Niyogi, U. K., Sabharwal, S. and Singh, G., Breathability studies of electron beam curable polyurethane pressure sensitive adhesive for bio-medical application.Radiat. Phys. Chem., 2014, 103, 75-83.
- Singh, A. K., Mehra, D. S., Niyogi, U. K., Sabharwal, S. and Singh, G., Life performance evaluation of electron beam-curable polyurethane pressure-sensitive adhesive tape for medical applications.J. Adhes. Sci. Technol., 2014, 28(12), 1192–1206.
- Fournier, E., Passirani, C., Montero-Menei, C. N. and Benoit, J. P., Biocompatibility of implantable synthetic polymeric drug carriers: focus on brain biocompatibility. Biomater, 2003, 24(19), 3311–3331.
- Lebowitz, M. D., Key concepts: chemical sensitization. In Multiple Chemical Sensitivities, National Academic Press, Washington, 1992.
- Turner-Warwick, M., On observing patterns of airflow obstruction in chronic asthma. Br. J. Dis. Chest., 1977, 71, 73–86.
- Berg, T., Boman, D. and Seglen, P. O., Induction of tryptophan oxidase in primary rat liver cell suspensions by glucocorticoid hormone. Ex. Cell Res., 1972, 72, 571–574.
- Edmondson, J. M., Armstrong, L. S. and Martinez, A. O., A rapid and simple MTT-based spectrophotometric assay for determining drug sensitivity in monolayer cultures. J. Tiss. Cult. Meth., 1988, 11, 15–17.
- Mosmann, T., Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J.Immun. Method., 1983, 65, 55–63.
- Lonnroth, E.-C. and Dahl, J. E., Cytotoxicity of dental glass ionomers evaluated using dimethylthiazol diphenyltetrazolium and neutral red tests. Acta. Odontol. Scand., 2001, 59, 34–39.
- Lonnroth, E.-C. and Dahl, J. E., Cytotoxicity of liquids and powders of chemically different dental materials using dimethylthiazol diphenyltetrazolium and neutral red tests. Acta. Odontol. Scand., 2003, 61, 52–56.
- Borenfreund, E. and Puerner, J. A., A simple quantitive procedure using monolayer cultures for cytotoxicity assays. J. Tissue Cult. Methods, 1984, 1, 7–9.
- Wennberg, A., In vitro assessment of the biocompatibility of dental materials – the Millipore filter method. J. Int. End., 1988, 21, 1–5.
- Lönnroth, E. C., Toxicity of medical glove materials: a pilot study. Int. J. Occup. Saf. Ergo., 2005, 11(2), 131–139.
- Matsuzaki, A., Yamashita, M. and Hara, N., Effect of pretreatment film composition on adhesion of organic film on zinc coated steel sheet. Mater. Trans., 2010, 51(10), 1833–1841.
- Amaral, A., Roos, A., Asua, J. M. and Creton, C., Assessing the effect of latex particle size and distribution on the rheological and adhesive properties of model waterborne acrylic pressure-sensitive adhesives films. J. Colloid Inter. Sci., 2005, 281, 325–338.
- Park, S., Adam Strömstedt, A. A. and Göransson, U., Cyclotide structure–activity relationships: qualitative and quantitative approaches linking cytotoxic and anthelmintic activity to the clustering of physicochemical forces. PLoS ONE, 2014, 9(3), e91430.
- Lee, Y. J., Lee, G., Kang, S. W., Cheong, Y. and Park, Y.-K., Label-free and quantitative evaluation of cytotoxicity based on surface nanostructure and biophysical property of cells utilizing AFM. Micron, 2013, 49, 54–59.
- Neilson, L., Mankus, C., Thorne, D., Jackson, D., DeBay, J. and Meredith, C., Development of an in vitro cytotoxicity model for aerosol exposure using 3D reconstructed human airway tissue; application for assessment of e-cigarette aerosol. Toxicol. In Vitro, 2015, 29(7), 1952–1962.
- McNamara, K., Kolaj-Robin, O., Belochapkine, S., Laffir, F., Gandhi, A. A. and Tofail, S. A. M., Surface chemistry and cytotoxicity of reactively sputtered tantalum oxide films on NiTi plates. Thin Solid Films, 2015, 589, 1–7.
- Geertsma, R. E., Orzechowski, T. J. H., Jonker, M., Dorpema, J. W. and Asten, J. A. A. M., Radiation vulcanized natural rubber latex: safer than conventionally processed latex? (RIVM report 605148007). Bilthoven, The Netherlands: National Institute for Public Health and the Environment, 1996.
- Cory, A. H., Owen, T. C., Barltrop, J. A. and Cory, J. G., Use of an aqueous tetrazolium/formazan assay for cell growth assays in culture. Cancer Commun., 1991, 3, 207–212.
- Lupu, A. R. and Popescu, T., The noncellular reduction of MTT tetrazolium salt by TiO2 nanoparticles and its implications for cytotoxicity assays. Toxicol. In Vitro, 2013, 27(5), 1445–1450.
- Emter, R. and Natsch, A., A fast Resazurin-based live viability assay is equivalent to the MTT-test in the KeratinoSens assay. Toxicol. In Vitro, 2015, 29(4), 688–693.
- Ikarashi, Y., Toyoda, K., Oshawa, N., Uchima, T., Tsuchiya, T. and Kaniwa, M., Comparative studies by cell culture and in vivo implantation test on the toxicity of natural rubber latex materials. J. Biomed. Mat. Res., 1992, 26, 339–356.
- Draize J. H., Woodard, G. and Calvery, G. O., Methods for the study of irritation and toxicity of substances applied topically to the skin and mucous membranes. J. Pharm. Exp. Ther., 1944, 82, 377–390.
- Casas, J. W., Lewerenz, G. M., Rankin, E. A., Willoughby Sr, J. A., Blakeman, L. C., McKim Jr, K. P. and Coleman, In vitro human skin irritation test for evaluation of medical device extracts. Toxicol. In Vitro, 2013, 27(8), 2175–2183.
- Pan, T.-L., Wang, P.-W., Aljuffali, I. A., Leu, Y.-L., Hung, Y.-Y. and Fang, J.-Y., Coumarin derivatives, but not coumarin itself, cause skin irritation via topical delivery. Toxicol. Lett., 2014, 226(2), 173–181.
- Piroird, C., Ovigne J.-M., Rousset, F., Martinozzi-Teissier, S., Gomes, C., Cotovio, J. and Alépée, L., The myeloid U937 skin sensitization test (U-SENS) addresses the activation of dendritic cell event in the adverse outcome pathway for skin sensitization. Toxicol. In Vitro, 2015, 29(5), 901–916.
- Urbisch, D. et al., Assessing skin sensitization hazard in mice and men using non-animal test methods. Regul. Toxicol. Pharmacol., 2015, 71(2), 337–351.
- Reisinger, K. et al., Systematic evaluation of non-animal test methods for skin sensitisation safety assessment. Toxicol. In Vitro, 2015, 29(1), 259–270.
- Nukada, Y., Ashikaga, T., Miyazawa, M., Hirota, M., Sakaguchi, H., Sasa, H. and Nishiyama, N., Prediction of skin sensitization potency of chemicals by human Cell Line Activation Test (h-CLAT) and an attempt at classifying skin sensitization potency. Toxicol. In Vitro, 2012, 26(7), 1150–1160.
- Viable Feedstock Options and Technological Challenges for Ethanol Production in India
Abstract Views :264 |
PDF Views:82
Authors
Affiliations
1 Shriram Institute for Industrial Research, 19, University Road, Delhi 110 007, IN
1 Shriram Institute for Industrial Research, 19, University Road, Delhi 110 007, IN
Source
Current Science, Vol 111, No 5 (2016), Pagination: 815-822Abstract
Though improvements in processing and technology are important, the fluctuating price of inputs such as molasses, corn, sugar beet, sugarcane, sweet sorghum, starch, etc. and their seasonal availability play an important role in ethanol industry. As a matter of fact, the ethanol industry based on conventional resources has reached its saturation point. Technologies for ethanol production from lignocellulosics are being developed by scientists world over with the objective of exploiting the potential of a resource, which is otherwise considered a waste, to generate energy. The focus has been to produce ethanol in a cost-effective manner, besides aiming to find use of its by-products as food supplements for cattles, etc. Recent developments like adoption of technologies such as dry grind fractionation, which is now commercially viable, would reduce the cost of milling; wet milling being cost-intensive and dry milling requiring smaller plants.Keywords
Ethanol, Feedstock, Lignocellulosics, Molasses, Sugarcane.- Soil Organic Carbon Stock in Agroforestry Systems in Western and Southern Plateau and Hill Regions of India
Abstract Views :278 |
PDF Views:94
Authors
Ram Newaj
1,
O. P. Chaturvedi
1,
Dhiraj Kumar
1,
Rajendra Prasad
1,
R. H. Rizvi
1,
Badre Alam
1,
A. K. Handa
1,
S. B. Chavan
1,
Anil Kumar Singh
1,
Mayank Chaturvedi
1,
P. S. Karmakar
1,
Abhishek Maurya
1,
Abhishek Saxena
1,
Gargi Gupta
1,
Kedari Singh
1
Affiliations
1 ICAR-Central Agroforestry Research Institute, Jhansi 284 003, IN
1 ICAR-Central Agroforestry Research Institute, Jhansi 284 003, IN
Source
Current Science, Vol 112, No 11 (2017), Pagination: 2191-2193Abstract
The rising level of carbon dioxide (CO2) in the atmosphere is a major concern, as scientific evidences show that it is the primary cause of global warming. CO2 concentration is expected to double by the middle or end of the 21st century, with a temperature rise between 1.5°C and 4.5°C (ref. 1). The importance of agroforestry as a land-use system is receiving wider recognition not only in terms of agricultural sustainability, but also in issues related to carbon sequestration or climate change.References
- Smith, K. A., Ball, T., Conen, F., Dobbie, K. E., Massheder, J. and Rey, A., Eur. J. Soil Sci., 2003, 54, 779–791.
- Verma, K. S., Kumar, S. and Bhardwaj, D. R., J. Tree Sci., 2008, 27(1), 14–27.
- Jordan, C. F., Agrofor. Syst., 2004, 61, 79–90.
- Peichl, M., Thevathasan, N. V., Gordon, A. M., Huss, J. and Abohassan, R. A., Agrofor. Syst., 2006, 66, 243–257.
- Lorenz, K. and Lal, R., Agron. Sustain. Dev., 2014, 34, 443–454.
- Nair, P. K. R., Agrofor. Syst., 2012, 86, 243–253.
- Haile, S. G., Nair, V. D. and Nair, P. K. R., Global Change Biol., 2010, 16, 427–438.
- Upson, M. A. and Burgess, P. J., Plant Soil, 2013, 373, 43–58.
- Walkley, A. J. and Black, C. A., Soil Sci., 1934, 37, 29–38.
- Soto-Pinto, L., Anzueto, M., Mendoza, J., Ferrer, G. J. and de Jong, B., Agrofor. Syst., 2010, 78, 39–51.
- Nair, P. K. R. and Nair, V. D., Curr. Opin. Environ. Sustain., 2014, 6, 22–27.
- Hendrick, R. L. and Pregitzer, K. S., J. Ecol., 1996, 84, 167–176.
- Martin, M. P., Wattenbach, M., Smith, P., Meersmans, J., Jolivet, C., Boulonne, L. and Arrouays, D., Biogeosciences, 2011, 8, 1053–1065.
- Munoz-Rojas, M., Jordan, A., Zavala, L. M., De la Rosa, D., Abd-Elmabod, S. K. and Anaya-Romero, M., Solid Earth, 2012, 3, 375–386.
- Swamy, S. L. and Puri, S., Agrofor. Syst., 2005, 64, 181–195.
- Controlled Hydrolytic Degradation of Polyglycolide–Caprolactone-Based Bioabsorbable Copolymer
Abstract Views :229 |
PDF Views:75
Authors
Affiliations
1 Material Science Division, Shriram Institute for Industrial Research, 19-University Road, Delhi 110 007, IN
1 Material Science Division, Shriram Institute for Industrial Research, 19-University Road, Delhi 110 007, IN
Source
Current Science, Vol 113, No 07 (2017), Pagination: 1354-1360Abstract
Polyglycolide–caprolactone (PGCL)-based copolymer was synthesized from glycolide and caprolactone by ring opening polymerization in the presence of stannous octoate catalyst and diethylene glycol initiator. The effects of prepolymerization time, monomer ratio, monomer-to-catalyst and monomer-to-initiator ratios on per cent weight conversion were optimized. The end-capped copolymer was synthesized to make absorbable sutures having controlled bioabsorbability at different pH levels. It was observed that endcapped absorbable copolymer was more stable at pH 10.0 compared to uncapped absorbable material. End-capped copolymer also retained higher tensile strength compared to uncapped copolymer after 21 days. This phenomenon of controlled hydrolytic degradation of PGCL-based bioabsorbable polymer having terminal group end-capping can be attributed to less availability of hydrophilic end groups facilitating hydrolytic degradation of polymers.Keywords
Biocompatibility, Bioabsorbable Copolymer, Hydrolytic Degradation, Polyglycolide–Caprolactone, Suture.References
- Gilding, D. K. and Reed, A. M., Biodegradable polymers for use in surgery – polyglycolic/poly(actic acid) homo- and copolymers: 1. Polymer, 1979, 20, 1459–1464.
- Deasy, P. B., Finan, M. P. and Meegan, M. J., Synthesis and characterization of poly(D,L-lactide-co-glycolide) copolymer. J. Microencapsulation, 1989, 6(3), 369–378.
- Chu, C. C. and Moncrief, G., An in vitro evaluation of the stability of mechanical properties of surgical suture materials in various pH conditions. Ann. Surg., 1983, 198(2), 223–228.
- Chu, C. C., A comparison of the effect of pH on the biodegradation of two synthetic absorbable sutures. Ann. Surg., 1982, 195, 55–59.
- Chu, C. C., Mechanical properties of suture materials: an important characterization. Ann. Surg., 1981, 193, 365–367.
- Dawkins, J. V., Denyer, R. and Maddock, J. W., Molecular weights by gel permeation chromatography: unperturbed dimensions calibration for polyisoprene. Polymer, 1969, 10, 154–158.
- Kim, C. W., Talac, R., Lu, L., Moore, M. J., Currier, B. L. and Yaszemski, M. J., Characterization of porous injectable poly(propylene fumarate)-based bone graft substitute. J. Biomed. Mater. Res. Part A, 2008, 85, 1114–1119.
- Young, S. et al., Accelerating bone generation and bone mineralization in the interparietal sutures of rats using an rhBMP-2/ACS composite after rapid expansion. Tissue Eng. Part A, 2009, 15, 2347–2362.
- Chellamani, K. P., Veerasubramanian, D. and Vignesh Balaji, R. S., Implantable medical textiles: synthetic suture manufacturing technology. J. Acad. Indust. Res., 2014, 3(2), 67–72.
- Gupta, V. B. and Kothari, V. K., Manufactured Fibre Technology, Chapman and Hall, London, 1997, 1st edn, pp. 31–66.
- Gogoi, R., Sarwar Alam, M. and Khandal, R. K., Effect of reaction time on the synthesis and properties of isocyanate terminated polyurethane prepolymer. Int. J. Eng. Res. Technol., 2014, 3(5), 1404–1411.
- Haesslein, A. et al., Long-term release of fluocinolone acetonide using biodegradable fumarate-based polymers. J. Controlled Rel., 2006, 114, 251–260.
- Ueda, H. et al., Injectable, in situ forming poly(propylene fumarate)based ocular drug delivery systems. J. Biomed. Mater. Res. Part A, 2007, 83, 656–666.
- Hacker, M. C. et al., Effect of drying history on swelling properties and cell attachment to oligo(poly(ethylene glycol) fumarate) hydrogels for guided tissue regeneration applications. J. Biomed. Mater. Res. Part A, 2009, 88, 976–989.
- Lee, K.-W., Wang, S., Yaszemski, M. J. and Lu, L., Physical properties and cellular responses to crosslinkable poly(propylene fumarate)/hydroxyapatite nanocomposites. Biomaterials, 2008, 29, 2839–2848.
- Jayabalan, M., Shalumon, K. T., Mitha, M. K., Ganesan, K. and Epple, M., Acta effect of calcium precursors and pH on the precipitation of carbonated hydroxyapatite. Biomaterialia, 2010, 6, 763–775.
- Lee, K.-W., Wang, S., Dadsetan, M., Yaszemski, M. J. and Lu, L., Enhanced cell in growth and proliferation through threedimensional nanocomposite scaffolds with controlled pore structures. Biomacromolecules, 2010, 11, 682–689.
- Mistry, A. S., Mikos, A. G. and Jansen, J. A., Degradation and biocompatibility of a poly(propylene fumarate)-based/alumoxane nanocomposite for bone tissue engineering. J. Biomed. Mater. Res. Part A, 2007, 83, 940–953.
- Mistry, A. S., Cheng, S. H., Yeh, T., Christenson, E., Jansen, J. A. and Mikos, A. G., Fabrication and in vitro degradation of porous fumarate-based polymer/alumoxane nanocomposite scaffolds for bone tissue engineering. J. Biomed. Mater. Res. Part A, 2009, 89, 68–79.
- Mistry, A. S., Pham, Q. P., Schouten, C., Yeh, T., Christenson, E. M., Mikos, A. G. and Jansen, J. A., In vivo bone biocompatibility and degradation of porous fumarate-based polymer/alumoxane nanocomposites for bone tissue engineering. J. Biomed. Mater. Res. Part A, 2010, 92, 451–462.
- Danti, S., D’Alessandro, D., Pietrabissa, A., Petrini, M. and Berrettini, S., Development of tissue-engineered substitutes of the ear ossicles: PORP-shaped poly(propylene fumarate)-based scaffolds cultured with human mesenchymal stromal cells. J. Biomed. Mater. Res. Part A, 2010, 92, 1343–1356.
- Nguyen, C., Young, S., Kretlow, J. D., Mikos, A. G. and Wong, M. A., composite critical-size rabbit mandibular defect for evaluation of craniofacial tissue regeneration. J. Oral Maxillofacial Surg.. 2011, 69, 11–18.
- Rosen, H. B., Chang, J., Wnek, G. E., Linhardt, R. J. and Langer, R., Bioerodible polyanhydrides for controlled drug delivery. Biomaterials, 1983, 4, 131–133.