Tasnuva Tamanna
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Tasnuva Tamanna has a total of 24 co-authors. Here are the top co-authors by number of shared publications:
- Aimin Yu
Department of Chemistry and Biotechnology, Swinburne University of Technology, Hawthorn, VIC 3122, Australia
7 shared publications - Cornelia Barbara Landersdorfer
Drug Delivery, Disposition, and Dynamics Theme, Monash Institute of Pharmaceutical Sciences, Monash University, 381 Royal Pde, Parkville, VIC, 3052, Australia
2 shared publications - Guosong Lai
Hubei Key Laboratory of Pollutant Analysis & Reuse Technology, College of Chemistry and Chemical Engineering, Hubei Normal University, Huangshi, China
2 shared publications - Jurgen Bernd Bulitta
St. Jude Children’s Research Hospital
2 shared publications - Li Fu
College of Materials and Environmental Engineering, Hangzhou Dianzi University, Hangzhou, China
2 shared publications - Abdul Khaliq
College of Engineering, University of Ha’il, Ha’il P.O. Box 2440, Saudi Arabia
1 shared publication
Latest Publications
- 1 February 2020
- Published by Elsevier in Journal of Colloid and Interface Science
- Vol. 560, 572-580
Tunable morphological changes of asymmetric titanium nanosheets with bactericidal properties
- 1 February 2020
- Published by Elsevier in Journal of Colloid and Interface Science
- Vol. 560, 572-580
Tunable morphological changes of asymmetric titanium nanosheets with bactericidal properties
- 24 May 2018
- Published by Springer Nature in Applied Nanoscience
- Vol. 8 (6) , 1471-1482
Prolonged and continuous antibacterial and anti-biofilm activities of thin films embedded with gentamicin-loaded mesoporous silica nanoparticles
- 24 May 2018
- Published by Springer Nature in Applied Nanoscience
- Vol. 8 (6) , 1471-1482
Prolonged and continuous antibacterial and anti-biofilm activities of thin films embedded with gentamicin-loaded mesoporous silica nanoparticles
- 17 May 2017
- Published by Royal Society of Chemistry (RSC) in Biomaterials Science
- Vol. 5 (7) , 1204-1229
Recent progress in the biomedical applications of polydopamine nanostructures
An overview of polydopamine derived nanostructures; PDA NPs, capsules, core-shell nanostructures and PDA coatings as well as their application in various biomedical fields.
- 17 May 2017
- Published by Royal Society of Chemistry (RSC) in Biomaterials Science
- Vol. 5 (7) , 1204-1229
Recent progress in the biomedical applications of polydopamine nanostructures
An overview of polydopamine derived nanostructures; PDA NPs, capsules, core-shell nanostructures and PDA coatings as well as their application in various biomedical fields.
- 2 December 2015
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 5 (130) , 107839-107846
Stability and controlled antibiotic release from thin films embedded with antibiotic loaded mesoporous silica nanoparticles
Thin films incorporated with gentamicin loaded mesoporous silica nanoparticles exhibit excellent stability and controlled release profile of the encapsulated antibiotic.
- 2 December 2015
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 5 (130) , 107839-107846
Stability and controlled antibiotic release from thin films embedded with antibiotic loaded mesoporous silica nanoparticles
Thin films incorporated with gentamicin loaded mesoporous silica nanoparticles exhibit excellent stability and controlled release profile of the encapsulated antibiotic.
- 11 February 2015
- Published by Springer Nature in Journal of Materials Science: Materials in Medicine
- Vol. 26 (2) , 1-7
Controlling antibiotic release from mesoporous silica nano drug carriers via self-assembled polyelectrolyte coating
Mesoporous silica nanoparticles (MSNs) have been explored as controlled drug delivery systems since the early 2000s, but many fundamental questions remain for this important application. We sought to design a pH controlled delivery system of gentamicin, an aminoglycoside antibiotic, based on MSNs. Under optimal conditions, MSN was able to load 219 µg gentamicin per mg MSNs. Polymeric networks encompassing gentamicin loaded MSNs were then established to tune the release kinetics. Embedding of drug pre-loaded MSNs was performed by an efficient layer-by-layer (LbL) self-assemble strategy using polystyrene sulfonate (PSS) and poly (allylamine hydrochloride) (PAH). We characterised the release kinetics by nonlinear mixed-effects modelling in the S-ADAPT software. The mean release time from uncoated MSNs was 3.6 days at pH 7.4 and 0.4 days at pH 1.4. A further slower release was achieved by diffusion through one or two PSS/PAH bilayer(s) which had a mean transit time of 6.0 days at pH 7.4 and 3.5 days at pH 1.4. The number of bilayers affected the shape of the release profile. The developed nano-drug carriers combined with the self-assembled polyelectrolyte coating allowed us to tune the release kinetics by pH and the number of bilayers.
- 11 February 2015
- Published by Springer Nature in Journal of Materials Science: Materials in Medicine
- Vol. 26 (2) , 1-7
Controlling antibiotic release from mesoporous silica nano drug carriers via self-assembled polyelectrolyte coating
Mesoporous silica nanoparticles (MSNs) have been explored as controlled drug delivery systems since the early 2000s, but many fundamental questions remain for this important application. We sought to design a pH controlled delivery system of gentamicin, an aminoglycoside antibiotic, based on MSNs. Under optimal conditions, MSN was able to load 219 µg gentamicin per mg MSNs. Polymeric networks encompassing gentamicin loaded MSNs were then established to tune the release kinetics. Embedding of drug pre-loaded MSNs was performed by an efficient layer-by-layer (LbL) self-assemble strategy using polystyrene sulfonate (PSS) and poly (allylamine hydrochloride) (PAH). We characterised the release kinetics by nonlinear mixed-effects modelling in the S-ADAPT software. The mean release time from uncoated MSNs was 3.6 days at pH 7.4 and 0.4 days at pH 1.4. A further slower release was achieved by diffusion through one or two PSS/PAH bilayer(s) which had a mean transit time of 6.0 days at pH 7.4 and 3.5 days at pH 1.4. The number of bilayers affected the shape of the release profile. The developed nano-drug carriers combined with the self-assembled polyelectrolyte coating allowed us to tune the release kinetics by pH and the number of bilayers.
- 12 February 2014
- Published by Taylor & Francis in Materials and Manufacturing Processes
- Vol. 29 (9) , 1030-1036
Nanocomposite Coating of Multilayered Carbon Nanotube–Titania
In this paper, we report a multiwalled carbon nanotube (MWCNT)/TiO2 composite film fabricated via a solution-based layer-by-layer self-assembly technique. The thin film deposition procedure was recorded by a UV/Vis spectrometer, which showed a linear increasing of absorbance with the bilayer number. X-ray diffraction analysis confirmed the formation of anatase titania after heat treatment. The enhanced photocatalytic property of the composite thin film was evaluated by its capacity to degrade rhodamine B under the UV radiation. Compared with TiO2 thin film, the MWCNT/TiO2 composite film showed a much higher photocatalytic performance. A 30 bilayer composite thin film (ca. 0.24 mg catalyst) was capable of completely degrading 10 mL of 2 mg/L Rh B solution within 5 h. The results also indicated that the hybrid catalyst could be reused for several cycles.
- 12 February 2014
- Published by Taylor & Francis in Materials and Manufacturing Processes
- Vol. 29 (9) , 1030-1036
Nanocomposite Coating of Multilayered Carbon Nanotube–Titania
In this paper, we report a multiwalled carbon nanotube (MWCNT)/TiO2 composite film fabricated via a solution-based layer-by-layer self-assembly technique. The thin film deposition procedure was recorded by a UV/Vis spectrometer, which showed a linear increasing of absorbance with the bilayer number. X-ray diffraction analysis confirmed the formation of anatase titania after heat treatment. The enhanced photocatalytic property of the composite thin film was evaluated by its capacity to degrade rhodamine B under the UV radiation. Compared with TiO2 thin film, the MWCNT/TiO2 composite film showed a much higher photocatalytic performance. A 30 bilayer composite thin film (ca. 0.24 mg catalyst) was capable of completely degrading 10 mL of 2 mg/L Rh B solution within 5 h. The results also indicated that the hybrid catalyst could be reused for several cycles.
- 7 January 2014
- Published by American Chemical Society (ACS) in Analytical Chemistry
- Vol. 86 (3) , 1789-1793
Ultrasensitive Immunoassay Based on Electrochemical Measurement of Enzymatically Produced Polyaniline
A novel ultrasensitive immunoassay method was developed based on the electrochemical measurement of polyaniline, which was catalytically produced by horseradish peroxidase-functionalized gold nanoparticle (HRP-Au NP) probe at an immunosensor. The immunosensor was prepared step-wise by first modifying the electrode with reduced graphene oxide (rGO)/Au NPs nanocomposite followed by the immobilization of capture antibodies on its surface. After performing a sandwich immunoreaction, the quantitatively captured HRP-Au NP nanoprobes could catalyze oxidation of aniline to produce electroactive polyaniline on the immunosensor surface. The electrochemical measurement of polyaniline enabled a novel detection strategy for HRP-based immunoassay. Both the signal amplification of the HRP-Au NP nanoprobe and the electron transfer acceleration of rGO/Au NPs on the immunosensor surface greatly improved the detection sensitivity of the immunoassay method. With the use of human IgG as a model analyte, this method showed a wide linear range over 4 orders of magnitude with a detection limit of 9.7 pg/mL. In addition, the immunosensor had low cost, satisfactory reproducibility and stability, and acceptable reliability. The relatively positive potential range for the polyaniline measurement completely excluded the conventional interference from dissolved oxygen. Thus, this method provides a promising potential for practical applications.
- 7 January 2014
- Published by American Chemical Society (ACS) in Analytical Chemistry
- Vol. 86 (3) , 1789-1793
Ultrasensitive Immunoassay Based on Electrochemical Measurement of Enzymatically Produced Polyaniline
A novel ultrasensitive immunoassay method was developed based on the electrochemical measurement of polyaniline, which was catalytically produced by horseradish peroxidase-functionalized gold nanoparticle (HRP-Au NP) probe at an immunosensor. The immunosensor was prepared step-wise by first modifying the electrode with reduced graphene oxide (rGO)/Au NPs nanocomposite followed by the immobilization of capture antibodies on its surface. After performing a sandwich immunoreaction, the quantitatively captured HRP-Au NP nanoprobes could catalyze oxidation of aniline to produce electroactive polyaniline on the immunosensor surface. The electrochemical measurement of polyaniline enabled a novel detection strategy for HRP-based immunoassay. Both the signal amplification of the HRP-Au NP nanoprobe and the electron transfer acceleration of rGO/Au NPs on the immunosensor surface greatly improved the detection sensitivity of the immunoassay method. With the use of human IgG as a model analyte, this method showed a wide linear range over 4 orders of magnitude with a detection limit of 9.7 pg/mL. In addition, the immunosensor had low cost, satisfactory reproducibility and stability, and acceptable reliability. The relatively positive potential range for the polyaniline measurement completely excluded the conventional interference from dissolved oxygen. Thus, this method provides a promising potential for practical applications.
- 1 January 2014
- Published by Springer Nature in Chemical Papers
- Vol. 68 (10) , 1283-1297
Chemical preparation and applications of silver dendrites
Silver dendrites have received immense attention because of their fascinating hierarchical structures and unique properties. Depending on the methods of synthesis, Ag dendrites can be implemented in numerous fields. This review summarizes a variety of Ag dendrites preparation techniques. The involved growth mechanisms are investigated in order to control the formation progress more effectively. With regard to the applications, this article mainly focuses on surface enhanced Raman spectroscopy, catalysis, superhydrophobic surface and surface enhanced fluorescence by using Ag dendrites. The remaining issues of the preparation methods, which impede the practical applications of Ag dendrites, are pointed out to enlighten their future research.
- 1 January 2014
- Published by Springer Nature in Chemical Papers
- Vol. 68 (10) , 1283-1297
Chemical preparation and applications of silver dendrites
Silver dendrites have received immense attention because of their fascinating hierarchical structures and unique properties. Depending on the methods of synthesis, Ag dendrites can be implemented in numerous fields. This review summarizes a variety of Ag dendrites preparation techniques. The involved growth mechanisms are investigated in order to control the formation progress more effectively. With regard to the applications, this article mainly focuses on surface enhanced Raman spectroscopy, catalysis, superhydrophobic surface and surface enhanced fluorescence by using Ag dendrites. The remaining issues of the preparation methods, which impede the practical applications of Ag dendrites, are pointed out to enlighten their future research.