Ziyaur Rahman

Prof. Ziyaur Rahman

Irma Lerma Rangel College of Pharmacy, Department of Pharmaceutical Sciences, Texas A&M Health Science Center, Texas A&M University, College Station, TX 77843, USA
orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 May 2020 in Drug Development and Industrial Pharmacy
Verified
Journal Article
Closed access
NCNaseem Charoo
Naseem Charoo
SASogra F. Barakh Ali
Sogra F. Barakh Ali
EMEman M. Mohamed
Eman M. Mohamed
MKMathew A. Kuttolamadom
Mathew A. Kuttolamadom
TOTanil Ozkan
Tanil Ozkan
Ziyaur RahmanZiyaur Rahman
Ziyaur Rahman
Food and Drug Administration (FDA) has approved a drug product (Spritam®) and many medical devices manufactured by 3-dimensional printing (3DP) processes for human use. There is immense potential to print personalized medicines using 3DP. Many 3DP methods have been reported in the literature for pharmaceutical applications. However, selective laser sintering (SLS) printing has remained least explored for pharmaceutical applications. There are many advantages and challenges in adopting a SLS method for fabrication of personalized medicines. Solvent free nature, availability of FDA approved thermoplastic polymer/excipients (currently used in hot melt-extrusion process), minimal/no post-processing step, etc. are some of the advantages of the SLS printing process. Major challenges of the technology are requirement of at least one thermoplastic component in the formulation and thermal stability of drug and excipients. This review provides an overview of the SLS printing method, excipient requirements, process monitoring, quality defects, regulatory aspects and potential pharmaceutical applications.

1 September 2010 in European Journal of Pharmaceutics and Biopharmaceutics
Verified
Journal Article
Closed access
Ziyaur RahmanZiyaur Rahman
Ziyaur Rahman
AZAhmed S. Zidan
Ahmed S. Zidan
Mansoor A. KhanMansoor A. Khan
Mansoor A. Khan

1 April 2010 in International Journal of Pharmaceutics
Verified
Journal Article
Closed access
Ziyaur RahmanZiyaur Rahman
Ziyaur Rahman
AZAhmed S. Zidan
Ahmed S. Zidan
MHMuhammad J. Habib
Muhammad J. Habib
Mansoor A. KhanMansoor A. Khan
Mansoor A. Khan

12 September 2018 in The AAPS Journal
Verified
Journal Article
Closed access
PDF file
Ziyaur RahmanZiyaur Rahman
Ziyaur Rahman
SASogra F. Barakh Ali
Sogra F. Barakh Ali
TOTanil Ozkan
Tanil Ozkan
NCNaseem Charoo
Naseem Charoo
IRIndra K. Reddy
Indra K. Reddy
MKMansoor A. Khan
Mansoor A. Khan

1 February 2012 in International Journal of Pharmaceutics
Verified
Journal Article
Closed access
NCNaseem Charoo
Naseem Charoo
ASAreeg A.A. Shamsher
Areeg A.A. Shamsher
AZAhmed S. Zidan
Ahmed S. Zidan
Ziyaur RahmanZiyaur Rahman
Ziyaur Rahman

1 May 2013 in Current Cancer Drug Targets
Verified
Journal Article
Closed access
PDF file
SASohail Akhter
Sohail Akhter
IAIqbal Ahmad
Iqbal Ahmad
Mohammad Zaki AhmadMohammad Zaki Ahmad
Mohammad Zaki Ahmad
FRFarshad Ramazani
Farshad Ramazani
ASAnjali Singh
Anjali Singh
RKRobbert J. Kok
Robbert J. Kok
As of 21st century, cancer is arguably the most complex and challenging disease known to mankind and an inevitable public health concern of this millennium. Nanotechnology, suitably amalgamated with cancer research, has ushered an era of highly personalized and safer medicines which can improve cancer diagnosis and therapy. A wide variety of nanomedicines are currently under investigation, including polymeric/non-polymeric nanoparticles, dendrimers, quantum dots, carbon nanotubes, lipid- and micelle-based nanoparticles. The bases of these nanomedicines in reducing toxicity associated with cancer therapy are their ability to carry a large payload and multivalent-ligand targeting. This imparts specificity for targeting the tissues as well as bypass resistance mechanisms. The major hurdles on these future medicines are potential toxicity of nanoparticles, which imposes the need of extensive regulatory evaluation before nanomedicines could be utilized as cancer therapeutics. This review highlights nanopharmaceuticals that have been investigated in oncology for various applications (diagnosis, therapeutic delivery and theranostics). It also discusses the effects of nano-sized materials on tissues/organ functions, the possibility of overcoming multi-drug resistance by using nanomedicines and their current clinical status.