Faculty Publications

Now showing 1 - 4 of 4

Faster Biomineralization and Tailored Mechanical Properties of Marine-Resource-Derived Hydroxyapatite Scaffolds with Tunable Interconnected Porous Architecture
(American Chemical Society service@acs.org, 2019) Hadagalli, K.; Panda, A.K.; Mandal, S.; Basu, B.
Although hydroxyapatite (HA)-based porous scaffolds have been widely researched in the last three decades, the development of naturally derived biomimetic HA with a tunable elastic modulus and strength together with faster biomineralization properties has not yet been achieved. To address this specific issue, we report here a scalable biogenic synthesis approach to obtain submicron HA powders from cuttlefish bone. The marine-resource-derived HA together with different pore formers can be conventionally sintered to produce physiologically relevant scaffolds with porous architecture. Depending on pore formers, the scaffolds with a range of porosity of up to 51% with a larger range of pore sizes up to 50 ?m were fabricated. An empirical relationship between the compression strength and the elastic modulus with fractional porosity was established. A combination of moderate compressive strength (12-15 MPa) with an elastic modulus up to 1.6 GPa was obtained from cuttlefish-bone-derived HA with wheat flour as the pore former. Most importantly, the specific HA scaffold supports the faster nucleation and growth of the biomineralized apatite layer with full coverage within 3 days of incubation in simulated body fluid. More importantly, the marine-species-derived HA supported better adhesion and proliferation of murine osteoblast cells than HA sintered using powders from nonbiogenic resources. The spectrum of physical and biomineralization properties makes cuttlefish-bone-derived porous HA a new generation of implantable biomaterial for potential application in cancellous bone regeneration. © 2019 American Chemical Society.
Hydroxyapatite—a promising sunscreen filter
(Springer, 2020) Pal, A.; Hadagalli, K.; Bhat, P.; Goel, V.; Mandal, S.
Exposure to ultraviolet (UV) radiation has been known to cause skin cancer, erythema, and sunburn. Continuous efforts have been made to make sunscreens more efficient and non-toxic. Inorganic sunscreens like TiO2 and ZnO are continued to be used for a few decades, and they are efficient in giving protection against harmful UV radiation, but they are photochemically active as well. They generate free radicals upon irradiation, which leads to reactive oxygen species (ROS) generation which is harmful to the human skin. Hydroxyapatite (HA) is a biocompatible material as it has a composition the same as the mineral content of the human bone; therefore, it is suitable for the dermatological application. Though HA itself does not provide protection against UV, studies on doped HA with various ions showed excellent performance. Pure HA absorbs only between 200 and 340 nm, with an intense band below 247 nm. HA doped with bivalent Zn2+, Fe2+, and trivalent Fe3+ and Cr3+, showed absorbance in the entire UV region. TiO2 provides absorbance in the entire UV range, while ZnO does so only in UVA. Compared to HA (refractive index, n = 1.6), TiO2 (n = 2.6) and ZnO (n = 1.9) have higher refractive index, which gives unwanted whitening effect. Additional properties can be brought in HA composites by adding material while retaining their individual properties. As HA is not photocatalytic, it does not lead to a generation of free radicals. This paper throws light on several aspects of HA-based sunscreen filters as an emerging future cosmetic material, and brief analysis and conclusions. © 2019, Australian Ceramic Society.
Effect of Fe3+ substitution on the structural modification and band structure modulated UV absorption of hydroxyapatite
(Blackwell Publishing Ltd, 2021) Hadagalli, K.; Shenoy, S.; Shakya, K.R.; Manjunath, G.; Tarafder, K.; Mandal, S.; Basu, B.
The effect of Fe3+ ionic substitution in hydroxyapatite (Ca10-xFex(PO4)6(OH)2) was studied using structural modifications, resulting in an improvement in UV absorption through a tailored optical band structure. Ca2+ of HA being larger compared to Fe3+ contributes to the shrinkage of the lattice. Undoped HA has a peak at 1085 cm?1 (?3 PO43?) which is shifted to 1033 cm?1 for Fe-HA, because of the perturbation in HA structure. An improvement of UV absorption in the entire UVA and UVB range with an increase in Fe content because of a decrease in bandgap from 5.9 eV to 2.1 eV with undoped and doped HA. Theoretically obtained band gap and optical behaviour of the systems are well correlated with the experimental findings. Moreover, the use of marine biowaste from cuttlefish bone, as the source of HA; low cost and promising UV absorption can have a potential application as UV protective sunscreen filters. © 2020 The American Ceramic Society
Preparation and structural characteristics of biphasic calcium phosphates from prawn shell bio-waste
(Taylor and Francis Ltd., 2023) Satish, P.; Salian, A.; Hadagalli, K.; Mandal, S.
The major objective of the work is to explore the mechanical properties of biphasic calcium phosphates (BCP), a biomaterial derived from marine resources like prawn (Fenneropenaeus Indicus) shell biowaste through wet chemical treatment of CaO. We report the BCP, a mixture of hydroxyapatite and octa calcium phosphate from prawn shell biowaste using wet chemical synthesis at 80°C under pH 10. XRD of BCP revealed the coexistence of secondary phases like β-TCP and α-TCP along with HA upon sintering at different temperatures. Furthermore, the SEM and EDS opened well-sintered uniaxial grains and the presence of trace elements like Fe, Mg, Si, and Na. The specimens sintered at 1100°C showed the highest compression strength of 56.8 MPa due to MgO at the grain boundaries, which plays an important role in grain boundary diffusion. Therefore, the prawn shell biowaste-derived BCP has good mechanical properties, making them suitable materials for high-strength bone substitutes. © 2023 Institute of Materials, Minerals and Mining. Published by Taylor & Francis on behalf of the Institute.

Faculty Publications

Browse

Filters

Settings

Sort By

Results per page

Search Results