Academic literature on the topic 'Parenteral drug delivery'

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Journal articles on the topic "Parenteral drug delivery"

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Gulati, Neha, and Himanshu Gupta. "Parenteral Drug Delivery: A Review." Recent Patents on Drug Delivery & Formulation 5, no. 2 (2011): 133–45. http://dx.doi.org/10.2174/187221111795471391.

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Collins-Gold, L. C., R. T. Lyons, and L. C. Bartholow. "Parenteral emulsions for drug delivery." Advanced Drug Delivery Reviews 5, no. 3 (1990): 189–208. http://dx.doi.org/10.1016/0169-409x(90)90016-l.

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Kwatra, Shubhika, Guncha Taneja, and Nimisha Nasa. "Alternative Routes of Drug Administration- Transdermal, Pulmonary & Parenteral." Indo Global Journal of Pharmaceutical Sciences 02, no. 04 (2012): 409–26. http://dx.doi.org/10.35652/igjps.2012.47.

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Oral Route is considered to be the most common route of drug delivery to obtain a systemic effect. However, with the recent developments in the field of drug delivery, it has been found that delivery through alternative routes is sometimes more beneficial. This article deals with the salient features, advantages and disadvantages of some of the alternative routes of drug administration- Transdermal, Pulmonary and Parenteral routes. Though the mechanisms of action of drugs delivered by these routes are different, they offer a common advantage- increased Therapeutic Index with simultaneously dec
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Chaubal, Mahesh V., and Theodore J. Roseman. "Drug delivery trends for parenteral therapeutics." Drug Delivery System 21, no. 4 (2006): 388–97. http://dx.doi.org/10.2745/dds.21.388.

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Neupane, Rabin, Sai H. S. Boddu, Mariam Sami Abou-Dahech, et al. "Transdermal Delivery of Chemotherapeutics: Strategies, Requirements, and Opportunities." Pharmaceutics 13, no. 7 (2021): 960. http://dx.doi.org/10.3390/pharmaceutics13070960.

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Chemotherapeutic drugs are primarily administered to cancer patients via oral or parenteral routes. The use of transdermal drug delivery could potentially be a better alternative to decrease the dose frequency and severity of adverse or toxic effects associated with oral or parenteral administration of chemotherapeutic drugs. The transdermal delivery of drugs has shown to be advantageous for the treatment of highly localized tumors in certain types of breast and skin cancers. In addition, the transdermal route can be used to deliver low-dose chemotherapeutics in a sustained manner. The transde
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Bulić, Matea, and Catherine Tuleu. "Rectal Drug Delivery to Paediatric Population." Hrvatski časopis zdravstvenih znanosti 1, no. 2 (2021): 76–80. http://dx.doi.org/10.48188/hczz.1.2.5.

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Despite its unpopularity, the rectal route of paediatric drug administration remains of interest especially in pre-school children as it can overcome some drug delivery challenges with oral and parenteral routes. Few studies have been conducted on the use and acceptability of traditional rectal dosage forms (i.e., suppositories, enemas and gels) in different parts of the world. It showed that barrier to adoption could be linked with poor knowledge, little information and understanding of this administration modality. Reformulation for the rectal delivery of drugs intended for oral and/or paren
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Haranath, Chinthaginjala. "Recent advances in lipid based nanovesicles for transdermal drug delivery." Journal of medical pharmaceutical and allied sciences 11, no. 6 (2022): 5375–81. http://dx.doi.org/10.55522/jmpas.v11i6.4273.

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Lipid based nanovesicles are the formulations which are used for the delivery of hydrophilic, hydrophobic and amphiphilic drugs or compounds. They are very helpful for the drugs which are hydrophilic and irritant drugs that can be encapsulated and delivered to the target site. They are very advantageous over conventional formulations. Lipid based nanovesicular systems will efficaciously help the drugs addressing the issues of solubility and penetration thereby promotes bioavailability. Now a days lipid based nanovesicles for transdermal delivery of drug has become very useful especially for hy
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Chavda, Vivek P., Shilpa Dawre, Anjali Pandya, et al. "Lyotropic liquid crystals for parenteral drug delivery." Journal of Controlled Release 349 (September 2022): 533–49. http://dx.doi.org/10.1016/j.jconrel.2022.06.062.

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Wissing, S. A., O. Kayser, and R. H. Müller. "Solid lipid nanoparticles for parenteral drug delivery." Advanced Drug Delivery Reviews 56, no. 9 (2004): 1257–72. http://dx.doi.org/10.1016/j.addr.2003.12.002.

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Anureet Arora, Manju Nagpal, and Geeta Aggarwal. "Microneedle Mediated Vaccine Delivery: A Comprehensive Review." Journal of Pharmaceutical Technology, Research and Management 5, no. 2 (2017): 163–84. http://dx.doi.org/10.15415/jptrm.2017.52011.

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Microneedles can be representative for paradigm shift of drug delivery from patient non-compliant parenteral injections to patient compliant drug delivery system, which can be utilized for administration of vaccines particularly along with macromolecular/micromolecular drugs. The concept of microneedles came into existence many decades ago but the use of microneedles to achieve efficient delivery of drugs into the skin became subject of research from mid of 1990’s. Various types of microneedles were utilized to enhance delivery of drugs and vaccines including solid microneedles for pre-treatme
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Dissertations / Theses on the topic "Parenteral drug delivery"

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Jørgensen, Lene. "Lipid based drug delivery systems for parenteral delivery of proteins /." Cph. : Department of Pharmaceutics, the Danish University of Pharmaceutical Sciences, 2004. http://www.dfh.dk/phd/defences/lenejoergensen.htm.

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Nugent, Josephine. "Design and delivery of non-parenteral vaccines." Thesis, Queen's University Belfast, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.337026.

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Babu, Kavitha Mary Vadakkel. "The Development of a Novel Controlled Release Drug Delivery System." The University of Waikato, 2007. http://hdl.handle.net/10289/2590.

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The aim of this research was to formulate, characterise and assess the feasibility of a novel drug delivery system known as the in situ gelling matrix (ISGM) where a hydrophilic polymer is suspended in a non-aqueous solvent that converts into a gel when injected subcutaneously or intramuscularly thus giving a controlled release matrix for a drug. Although the concept has been patented with claims that this kind of drug delivery is achievable in theory for a wide variety of candidate substances, actual formulation studies for making a commercially viable product for this technology are complet
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Lance, Martin Richard. "Formulation and evaluation of novel amphotericin B oil/water triglyceride emulsions." Thesis, University of Nottingham, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.338440.

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Krenzlin, Stefanie [Verfasser]. "Challenging controlled drug delivery : matrix systems for oral and parenteral application / Stefanie Krenzlin." Berlin : Freie Universität Berlin, 2012. http://d-nb.info/1027816118/34.

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Besslich, Lisa [Verfasser]. "Formulation and process development of biodegradable microparticles for controlled parenteral drug delivery / Lisa Beßlich." Berlin : Freie Universität Berlin, 2020. http://d-nb.info/1215572115/34.

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Beßlich, Lisa [Verfasser]. "Formulation and process development of biodegradable microparticles for controlled parenteral drug delivery / Lisa Beßlich." Berlin : Freie Universität Berlin, 2020. http://d-nb.info/1215572115/34.

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Meynell, Helen Mary. "Bacterial modulation of particle transport across the follicle-associated epithelium of Peyer's patches." Thesis, University of Nottingham, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.285656.

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Gomes, Rodrigues Alexandre [Verfasser]. "Parenteral controlled drug delivery by novel direct injectable polymer (DIPO) : in situ forming implant / Alexandre Gomes Rodrigues." Halle, 2018. http://d-nb.info/1160514518/34.

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MAGRI, GIULIA. "DEVELOPMENT OF NOVEL BIODEGRADABLE MATERIALS STABLE TO STERILIZATION FOR THE PREPARATION OF DRUG DELIVERY SYSTEMS." Doctoral thesis, Università degli Studi di Milano, 2019. http://hdl.handle.net/2434/607019.

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Poly(lactide-co-glycolide) [PLGA] is the most exploited biodegradable and biocompatible material in the pharmaceutical field for the preparation of long- acting parenteral formulations, despite there are limitations related to the PLGA itself or to the final product to face with. These mainly include the limited ability in encapsulating hydrophilic compounds, the physical and chemical instabilities in aqueous media, the detrimental effect of the sterilization methods and the drop off in the micro-environmental pH upon degradation. Hence, there is the need to find new strategies for their overc
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Books on the topic "Parenteral drug delivery"

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Dorati, Rossella. Copolymers in the preparation of parenteral drug delivery systems. Nova Science, 2010.

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D, Ensminger William, Selam Jean-Louis, and Drug Delivery System Symposium (1988 : Monaco, Monaco), eds. Update in drug delivery systems. Futura Pub., 1989.

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Wasan, Kishor M., ed. Role of Lipid Excipients in Modifying Oral and Parenteral Drug Delivery. John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0470097981.

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Peptide And Protein Drug Delivery (Advances in Parenteral Science). 2nd ed. Marcel Dekker Inc, 2006.

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Lee, Vincent. Peptide and Protein Drug Delivery (Advances in Parenteral Science, No 4). CRC, 1990.

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Wasan, Kishor M. Role of Lipid Excipients in Modifying Oral and Parenteral Drug Delivery: Basic Principles and Biological Examples. Wiley-Interscience, 2006.

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Wasan, Kishor M. Role of Lipid Excipients in Modifying Oral and Parenteral Drug Delivery: Basic Principles and Biological Examples. Wiley & Sons, Incorporated, John, 2006.

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Wasan, Kishor M. Role of Lipid Excipients in Modifying Oral and Parenteral Drug Delivery: Basic Principles and Biological Examples. Wiley & Sons, Incorporated, John, 2007.

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9

Ludwig, John D., and Sandeep Nema. Pharmaceutical Dosage Forms: Parenteral Medications, Third Edition. 3 Volume Set. Taylor & Francis Group, 2010.

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Book chapters on the topic "Parenteral drug delivery"

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Shahiwala, Aliasgar, Tejal A. Mehta, and Munira M. Momin. "Parenteral Drug Delivery Systems." In In-Vitro and In-Vivo Tools in Drug Delivery Research for Optimum Clinical Outcomes. CRC Press, 2018. http://dx.doi.org/10.1201/b22448-9.

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Bontempo, John A. "Parenteral Formulation for Peptides, Proteins, and Monoclonal Antibodies Drugs: A Commercial Development Overview." In Drug Delivery. John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471475734.ch15.

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Bose, Sagarika. "Parenteral Drug Delivery for Older Patients." In Developing Drug Products in an Aging Society. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-43099-7_18.

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Patel, Gayatri C. "Stimuli-Responsive Hydrogels for Parenteral Drug Delivery." In Functional Hydrogels in Drug Delivery. CRC Press, 2017. http://dx.doi.org/10.4324/9781315152271-9.

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Patel, Gayatri. "Stimuli-Responsive Hydrogels for Parenteral Drug Delivery." In Functional Hydrogels in Drug Delivery. CRC Press, 2017. http://dx.doi.org/10.1201/9781315152271-10.

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Rehman, Nahid, and Anjana Pandey. "Nanoparticle Application in Non-Parenteral Applications." In Engineered Nanoparticles as Drug Delivery Systems. CRC Press, 2022. http://dx.doi.org/10.1201/9781003252122-7.

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Vhora, Imran, Denish Bardoliwala, Saketh Reddy Ranamalla, and Ankit Javia. "Parenteral Controlled and Prolonged Drug Delivery Systems: Therapeutic Needs and Formulation Strategies." In Novel Drug Delivery Technologies. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-3642-3_7.

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Soo, Patrick Lim, Michael Dunne, Jubo Liu, and Christine Allen. "Nano-sized Advanced Delivery Systems as Parenteral Formulation Strategies for Hydrophobic Anti-cancer Drugs." In Nanotechnology in Drug Delivery. Springer New York, 2009. http://dx.doi.org/10.1007/978-0-387-77668-2_12.

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Lundholm, K. G., and A. Hyltander. "Long-Term and Home Parenteral Nutrition to Cancer Patients." In Drug Delivery in Cancer Treatment III. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75938-3_4.

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Wischke, C., and S. P. Schwendeman. "Degradable Polymeric Carriers for Parenteral Controlled Drug Delivery." In Fundamentals and Applications of Controlled Release Drug Delivery. Springer US, 2011. http://dx.doi.org/10.1007/978-1-4614-0881-9_8.

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Conference papers on the topic "Parenteral drug delivery"

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McGee, James K., Koby Kubrin, Adeel Ahmed, and Michael G. Schrlau. "3D Printed Carbon Nanotube Array Interface for In Vivo Drug Delivery." In ASME 2017 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/imece2017-71815.

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The development of gene therapies, small molecules and nanoparticle-based therapeutics in pharmacology have prompted the need for parenteral administration as they possess limited bioactivity, low stability, high specificity and potency. The ability to directly deliver drugs to a specific area offers the capability of minimized required drug quantity, localization of exposure, and limited systemic side effects. Currently, there is no standard for the creation of implantable devices to monitor health status and provide therapeutic treatment. We explored the applications and uses for carbon nano
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