Ahad Rahim
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Ahad Rahim has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Gail ter Haar
Division of Radiotherapy and Imaging, The Institute of Cancer Research, London SM2 5NG, UK
3 shared publications - Jeffrey Colin Bamber
Institute of Cancer Research
3 shared publications Sarah L. Taylor
Cell and Molecular Biology, Institute of Cancer Research, London, United Kingdom
3 shared publicationsColin D. Porter
The Institute of Cancer Research, Gene Therapy Group, Department of Cell and Molecular Biology, 237 Fulham Road, Chelsea, London SW3 6JB, UK
2 shared publicationsNigel L. Bush
The Institute of Cancer Research and The Royal Marsden NHS Trust, Joint Department of Physics, Downs Road, Sutton SM2 5PT, UK
2 shared publications- Colin D. Porter
The Institute of Cancer Research, Section of Cell and Molecular Biology, 237 Fulham Rd., London SW3 6JB, UK
1 shared publication
Latest Publications
- Open Access
- 31 December 2006
- Published by Elsevier in Molecular Therapy
- Vol. 13, S210
546. Targeted Non-Viral Gene Delivery Using Microbubbles and Focused Ultrasound
- 31 December 2006
- Published by Elsevier in Molecular Therapy
- Vol. 13, S210
Open Access546. Targeted Non-Viral Gene Delivery Using Microbubbles and Focused Ultrasound
- 18 September 2006
- Published by Wiley in The Journal of Gene Medicine
- Vol. 8 (11) , 1347-1357
Spatial and acoustic pressure dependence of microbubble‐mediated gene delivery targeted using focused ultrasound
Background: Ultrasound/microbubble‐mediated gene delivery has the potential to be targeted to tissue deep in the body by directing the ultrasound beam following vector administration. Application of this technology would be minimally invasive and benefit from the widespread clinical experience of using ultrasound and microbubble contrast agents. In this study we evaluate the targeting ability and spatial distribution of gene delivery using focused ultrasound.Methods: Using a custom‐built exposure tank, Chinese hamster ovary cells in the presence of SonoVue® microbubbles and plasmid encoding β‐galactosidase were exposed to ultrasound in the focal plane of a 1 MHz transducer. Gene delivery and cell viability were subsequently assessed. Characterisation of the acoustic field and high‐resolution spatial analysis of transfection were used to examine the relationship between gene delivery efficiency and acoustic pressure.Results: In contrast to that seen in the homogeneous field close to the transducer face, gene delivery in the focal plane was concentrated on the ultrasound beam axis. Above a minimum peak‐to‐peak value of 0.1 MPa, transfection efficiency increased as acoustic pressure increased towards the focus, reaching a maximum above 1 MPa. Delivery was microbubble‐dependent and cell viability was maintained.Conclusions: Gene delivery can be targeted using focused ultrasound and microbubbles. Since delivery is dependent on acoustic pressure, the degree of targeting can be determined by appropriate transducer design to modify the ultrasound field. In contrast to other physical gene delivery approaches, the non‐invasive targeting ability of ultrasound makes this technology an attractive option for clinical gene therapy. Copyright © 2006 John Wiley & Sons, Ltd.
- 18 September 2006
- Published by Wiley in The Journal of Gene Medicine
- Vol. 8 (11) , 1347-1357
Spatial and acoustic pressure dependence of microbubble‐mediated gene delivery targeted using focused ultrasound
Background: Ultrasound/microbubble‐mediated gene delivery has the potential to be targeted to tissue deep in the body by directing the ultrasound beam following vector administration. Application of this technology would be minimally invasive and benefit from the widespread clinical experience of using ultrasound and microbubble contrast agents. In this study we evaluate the targeting ability and spatial distribution of gene delivery using focused ultrasound.Methods: Using a custom‐built exposure tank, Chinese hamster ovary cells in the presence of SonoVue® microbubbles and plasmid encoding β‐galactosidase were exposed to ultrasound in the focal plane of a 1 MHz transducer. Gene delivery and cell viability were subsequently assessed. Characterisation of the acoustic field and high‐resolution spatial analysis of transfection were used to examine the relationship between gene delivery efficiency and acoustic pressure.Results: In contrast to that seen in the homogeneous field close to the transducer face, gene delivery in the focal plane was concentrated on the ultrasound beam axis. Above a minimum peak‐to‐peak value of 0.1 MPa, transfection efficiency increased as acoustic pressure increased towards the focus, reaching a maximum above 1 MPa. Delivery was microbubble‐dependent and cell viability was maintained.Conclusions: Gene delivery can be targeted using focused ultrasound and microbubbles. Since delivery is dependent on acoustic pressure, the degree of targeting can be determined by appropriate transducer design to modify the ultrasound field. In contrast to other physical gene delivery approaches, the non‐invasive targeting ability of ultrasound makes this technology an attractive option for clinical gene therapy. Copyright © 2006 John Wiley & Sons, Ltd.
- Open Access
- 1 August 2006
- Published by Elsevier in Ultrasound in Medicine & Biology
- Vol. 32 (8) , 1269-1279
Physical parameters affecting ultrasound/microbubble-mediated gene delivery efficiency in vitro
- 1 August 2006
- Published by Elsevier in Ultrasound in Medicine & Biology
- Vol. 32 (8) , 1269-1279
Open AccessPhysical parameters affecting ultrasound/microbubble-mediated gene delivery efficiency in vitro