Advanced Drug Delivery Systems in the Management of Cancer

Table of Contents

1. Introduction to cancer cell biology2. Current practice in cancer pharmacotherapy3. Current practices in oncology drug delivery4. Emerging need of advanced drug delivery systems in cancer5. Target drug delivery in cancer6. Material and strategies used in oncology drug delivery7. Hydrogel based drug delivery systems for cancer therapy8. Recent advances in drug formulation development for targeting lung cancer9. Advanced drug delivery systems in lung cancer10. Advanced drug delivery systems in breast cancer11. Advance drug delivery systems in the treatment of ovarian cancer12. Advanced drug delivery systems in blood cancer13. Advanced drug delivery systems in kidney cancer14. Advance drug delivery systems in glioblastoma15. Advanced drug delivery systems in prostate cancer16. Nanomedicine-based doxorubicin delivery for skin cancer with theranostic potential17. Advanced drug delivery systems in liver cancer18. Advanced drug delivery systems in hepatocellular carcinoma19. Advanced drug delivery systems in oral cancer20. Advance drug delivery system in pancreatic cancer21. Advanced drug delivery system in colorectal cancer22. Current strategies in targeted anticancer drug delivery systems to brain23. Neuroblastoma: Current advancements and future therapeutics24. Nanoparticulate systems and their translation potential for breast cancer therapeutics25. Advancement on nanoparticle-based drug delivery systems for cancer therapy26. Advances in polymeric nanoparticles for drug delivery systems in cancer: Production and characterization27. Lipid-polymer hybrid nanocarriers for delivering cancer therapeutics28. Advancements on microparticles-based drug delivery systems for cancer therapy29. Microparticles for cancer therapy30. Biosynthetic exosome nanoparticles isolation, characterization, and their diagnostic and therapeutic applications31. Advances in delivery of nanomedicines and theranostics for targeting breast cancer32. Bioresponsive nano-theranostics approaches for cancer targeting33. Two-dimensional materials-based nanoplatforms for lung cancer management: Synthesis, properties, and targeted therapy34. Cell and gene therapies Emerging technologies and drug delivery systems for treating brain cancer35. Targeting siRNAs in cancer drug delivery36. Targeting micro-ribonucleic acid (miRNA) in cancer using advanced drug delivery systems37. Organic nanocarriers for targeted delivery of anticancer agents38. Targeting cancer using phytoconstituents-based drug delivery39. Clinical trials in drug delivery for the treatment of cancer40. Future prospects and challenges in cancer drug delivery

Authors

Kamal Dua Senior Lecturer, Discipline of Pharmacy, Graduate School of Health, University of Technology Sydney, Sydney, NSW, Australia.

Dr. Kamal Dua is a Senior Lecturer in the Discipline of Pharmacy at the Graduate School of Health, University of Technology Sydney (UTS), Australia. He has research experience of over many years in the field of drug delivery systems targeting inflammatory diseases. Dr. Dua researches in two complementary areas; drug delivery and immunology, specifically addressing how these disciplines can advance one another, helping the community to live longer and healthier. This is evidenced by his extensive publication record in reputed journals. Dr. Dua's research interests focus on harnessing the pharmaceutical potential of modulating critical regulators such as Interleukins and microRNAs and developing new and effective drug delivery formulations for the management of chronic airway diseases. He has published more than 80 research articles in peer-reviewed international journals and authored or co-authored four books. He is an active member of many national and international professional societies.

Meenu Mehta Discipline of Pharmacy, Graduate School of Health, University of Technology Sydney, Sydney, NSW, Australia. Meenu Mehta is a research scholar at the Discipline of Pharmacy, Graduate School of Health, the University of Technology Sydney. Her research is focused in the area of pharmaceutical technologies developing novel drug delivery systems for chronic respiratory diseases such as asthma, chronic obstructive lung disease (COPD), and lung cancer. She has obtained her M. Pharm degree in Pharmaceutical
Sciences in India, where she has gained working experience in several areas such as drug development, analytical methods, pharmacognosy studies, microwave techniques, and nanotechnology-based novel drug delivery systems. Mehta has received various awards and carries an impressive bibliography of scientific papers published in journals of international repute. Terezinha de Jesus Andreoli Pinto School of Pharmaceutical Sciences, University of Sao Paulo, Sao Paulo, Brazil. Terezinha de Jesus Andreoli Pinto is a Professor at the School of Pharmaceutical Sciences, University of Sao Paulo. Professor Terezinha holds more than 40 years of sound experience in academia and researches on parenterals (formulation, analytical, microbiological, and performance methods) and medical devices. Professor Terezinha authored 180 articles in scientific journals, more than 12 book chapters and also holds two patents. Alongside her career, Professor Terezinha took on management roles in the University, such as being dean of School of Pharmacy for two mandates (2004-2008 and 2012-2016) and also being chair of Deliberative Board of FURP-a pharmaceutical firm that manufactures products from the WHO Essential Medicines list, run by Sao Paulo State Government. Strong scientific skills allied to leadership and management allowed her to establish agreements with internationally prestigious institutions including the University of Alberta, Lisbon, and Bath. Under her supervision, the CONFAR Laboratory was set up, the only Brazilian state university laboratory accredited by the National Institute of Metrology, Quality and Technology (INMETRO) (ISO/IEC 17025) and, authorized by the National Agency of Sanitary Surveillance (ANVISA) and the Ministry of Agriculture, Livestock, and Supplies (MAPA), and is considered a reference both in Brazil and overseas, in the analytical area. Professor Terezinha is also involved with standard-setting activities in agencies such as Brazilian Pharmacopeia (as coordinator of the Brazilian Pharmacopeia Drug Product and Medical Devices technical committee, and currently member of Biological and Biotechnological Products Committee), International Standard Organization (ISO) as Brazilian Association of Technical Norms (ABNT) representative and also the United States Pharmacopeia stakeholder with participation in convention current cycle. Lisa G. Pont Discipline of Pharmacy, Graduate School of Health, University of Technology Sydney, Sydney, NSW, Australia. Lisa G. Pont is a Professor in the Discipline of Pharmacy, Graduate School of Health at the University of Technology Sydney. Pont is a pharmacoepidemiologist with expertise in medicine utilization and health service research to evaluate, understand, and improve the quality and safety of medicine use in practice. Her research explores current practices and patterns of medicines use across populations with a focus on the safety and quality of prescribing and medicines use. Throughout her career, Professor Pont has received a number of awards including two national NPS MedicineWise awards in 2014 and in 2016 for her research. She is a registered pharmacist and was awarded the Society of Hospital Pharmacist of Australia Medal of Merit in 2018. Kylie A. Williams Discipline of Pharmacy, Graduate School of Health, University of Technology Sydney, Sydney, NSW, Australia. Kylie A. Williams is a pharmacist and academic leader. She is a founding member of the Graduate School of Health at University of Technology Sydney (UTS), where she is currently the Head of Pharmacy and the Deputy Head of School Learning & Teaching. She has over 25 years of academic experience in learning and teaching, curricula development, research, and academic leadership. Professor Williams leads a research team focused on development, implementation, and evaluation of new models of pharmacy and health service delivery. Alongside her research expertise, Professor Williams is internationally recognized for her curriculum development, and has received a number of teaching grants and awards and has coauthored numerous teaching-related peer-reviewed journal articles, professional books, and educational articles for pharmacists. Michael Rathbone ULTI Pharmaceuticals, Turangi, New Zealand. Michael J. Rathbone is founder and managing director of his own company, ULTI Pharmaceuticals, New Zealand. He is also an associate of the School, Discipline of Pharmacy, Graduate School of Health, University of Technology Sydney, NSW, Australia. He was formerly professor of Pharmaceutical Technology and dean, School of Pharmacy, International Medical University, Kuala Lumpur, Malaysia. Prior to this he was associate professor of Pharmaceutics, School of Pharmacy, Griffith University, Australia where his responsibilities included Acting Head of School. Previous to his appointment at Griffith University, he was the director of Research and General Manager InterAg, New Zealand, where he spearheaded the companies veterinary controlled drug delivery research and directed their national and global collaborative research activities. Dr. Rathbone obtained his undergraduate degree in Pharmacy at Leicester Polytechnic (De Montfort University), UK (1980), and PhD in Pharmaceutics from the University of Aston, Birmingham, UK (1986). Dr. Rathbone has innovated many novel veterinary drug delivery systems, several of which have been registered on the New Zealand, Australian and United States markets. He is a fellow of the Controlled Release Society, has served on the Board of Directors of the CRS and has received several prestigious awards for his contribution to the science and technology of controlled release. He has edited eight books in the area of modified release drug delivery and 10 special theme issues of journals such as Advanced Drug Delivery Reviews and Journal of Controlled Release. His knowledge of the entire spectrum of innovation, product research & development, cGMP analysis, manufacturing scale-up, QC analysis, stability testing, and registration provides him with an extensive overview, and unparalleled experience of the veterinary pharmaceutical industry.