Relevant bibliographies by topics / Drug solution

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Drug solution'

Author: Grafiati
Published: 5 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Drug solution"

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Shurshina, Anzhela, Roman Lazdin, Elena Zakharova, Anastasiya Titlova, and Elena Kulish. "Prolonging effect of polyvinyl alcohol on the drug release." Chimica Techno Acta 9, no. 2 (2022): 20229206. http://dx.doi.org/10.15826/chimtech.2022.9.2.06.

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Polymers are currently of interest as drug delivery systems. The use of polymeric forms of medicinal substances will eliminate or reduce the disadvantages of traditional drugs. The purpose of this work was to assess the ability to prolong the action of polyvinyl alcohol in relation to the drug release when going from dilute to more concentrated solutions. It was established that an increase in the viscosity of the polymer in solution caused by an increase in its concentration results not only in a slowdown in the diffusion of drugs from the polymer solution, but also in a significant decrease
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Scanga, Lisa. "Drug Problem: Environmental Solution." Pace Environmental Law Review 22, no. 1 (2005): 151. http://dx.doi.org/10.58948/0738-6206.1139.

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De Vin, Filip, Peter Rutherford, and Dirk Faict. "Intraperitoneal Administration of Drugs in Peritoneal Dialysis Patients: A Review of Compatibility and Guidance for Clinical Use." Peritoneal Dialysis International: Journal of the International Society for Peritoneal Dialysis 29, no. 1 (2009): 5–15. http://dx.doi.org/10.1177/089686080902900101.

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Peritoneal dialysis (PD) is an effective home-based therapy for end-stage renal failure. Intraperitoneal administration of drugs to PD patients is particularly important for the treatment of peritonitis. Clinicians need to know that the administered drug is compatible with both the PD solution and its container. A detailed literature search on drug compatibility and stability was performed and results of all published stability studies are presented for all drugs, PD solutions, and containers studied. These data will aid clinicians managing PD patients and provide a resource to demonstrate whi
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Odeh, Afnan Bany, Boushra El-Sayed, Matthias Manne Knopp, Thomas Rades, and Lasse Ingerslev Blaabjerg. "Influence of Polyvinylpyrrolidone Molecular Weight and Concentration on the Precipitation Inhibition of Supersaturated Solutions of Poorly Soluble Drugs." Pharmaceutics 15, no. 6 (2023): 1601. http://dx.doi.org/10.3390/pharmaceutics15061601.

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Supersaturating drug delivery systems such as solid dispersions of a drug in a polymer are frequently used in pharmaceutical development to enable oral delivery of poorly soluble drugs. In this study, the influence of the concentration and molecular weight of polyvinylpyrrolidone (PVP) on the precipitation inhibition of the poorly soluble drugs albendazole, ketoconazole and tadalafil is investigated to expand the understanding of the mechanism of PVP as a polymeric precipitation inhibitor. A three-level full-factorial design was used to delineate the influence of polymer concentration and visc
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Shi, Li, and Naixia Zhang. "Applications of Solution NMR in Drug Discovery." Molecules 26, no. 3 (2021): 576. http://dx.doi.org/10.3390/molecules26030576.

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During the past decades, solution nuclear magnetic resonance (NMR) spectroscopy has demonstrated itself as a promising tool in drug discovery. Especially, fragment-based drug discovery (FBDD) has benefited a lot from the NMR development. Multiple candidate compounds and FDA-approved drugs derived from FBDD have been developed with the assistance of NMR techniques. NMR has broad applications in different stages of the FBDD process, which includes fragment library construction, hit generation and validation, hit-to-lead optimization and working mechanism elucidation, etc. In this manuscript, we
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Chen, Pin, Xin Wang, Yan Dong, and Xiaohong Hu. "Development of a Layer-by-Layer Assembled Film on Hydrogel for Ocular Drug Delivery." International Journal of Polymer Science 2015 (2015): 1–9. http://dx.doi.org/10.1155/2015/535092.

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Hydrogel is a kind of attractive drug carriers because of its good biocompatibility and transparency. But traditional hydrogel showed some restrictions in its application in ocular drug delivery. A simple surface modification technique based on layer-by-layer (LbL) self-assembled multilayer for ocular drug delivery was developed in this work. Polycarboxymethyl-β-cyclodextrin (poly(CM-β-CD))/poly-l-lysine (PLL) multilayer film was designed and constructed for ocular drug delivery, sinceβ-CD showed good drug delivery property. The properties such as the contact angle and transparency varied a li
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Potts, Keagan. "A Solution to the Hard Problem of Soft Law." Michigan Journal of Environmental & Administrative Law, no. 10.2 (2021): 483. http://dx.doi.org/10.36640/mjeal.10.2.solution.

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Administrative Agencies often rely on guidance documents to carry out their statutory mandate. Over the past few decades, the Food and Drug Administration (FDA) has been criticized for using soft law guidance documents to exercise powers beyond those authorized by Congress. Since attacks on the use of guidance documents persist and agencies need soft law to respond quickly and flexibly to rapid technological growth, it is essential to develop a solution that preserves this crucial regulatory mechanism and prevents its abuse. The most likely alternative to soft law guidance is formal regulation
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Walicka, A., and B. Iwanowska-Chomiak. "Drug Diffusion Transport Through Human Skin." International Journal of Applied Mechanics and Engineering 23, no. 4 (2018): 977–88. http://dx.doi.org/10.2478/ijame-2018-0055.

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Abstract The stratum corneum (SC) forms the outermost layer of the human skin and is essentially a multilamellar lipid milieu punctuated by protein-filled corneocytes that augment membrane integrity and significantly increase membrane tortuosity. The lipophilic character of the SC, coupled with its intrinsic tortuosity, ensure that it almost always provides the principal barrier to the entry of drug molecules into the organism. Drugs can be administered either as suspensions or as solutions and the formulation can range in complexity from a gel or and ointment to a multilayer transdermal path.
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Almakaeva, LG, LG Naumenok, NV Begunova, VG Dolya, and MS Almakaev. "DEVELOPMENT OF DOMESTIC INFUSION DRUGS BASED ON PARACETAMOL." Annals of Mechnikov Institute, no. 2 (November 18, 2016): 65–68. https://doi.org/10.5281/zenodo.167497.

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The intravenous form of paracetamol compared with oral more reliably supports effective drug concentration in blood plasma that promotes a higher therapeutic effect. Recent studies have confirmed that the use of the intravenous form of paracetamol to deal with postoperative pain multimodal analgesia modes results in reducing the frequency and quantity of opioids administered , and, as a consequence, its associated side effects. The drug Paracetamol , infusion solution 10 mg / ml to 100 ml glass bottles is a drug - generic . His qualitative and quantitative composition is developed from the stu
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Gomez-Sanchez, Ruben, Stephen Besley, Zoe Zeliku, and Robert J. Young. "Method Development and Application of an Accelerated Solution Stability Screen for Drug Discovery." SLAS DISCOVERY: Advancing the Science of Drug Discovery 25, no. 10 (2020): 1191–96. http://dx.doi.org/10.1177/2472555220931795.

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An important aspect to understand about an experimental molecule in drug discovery is its stability in solution. A compound that degrades might be eliciting its apparent effect via a degradation product, so it is important to understand the solution stability profile of a compound early on in the drug discovery process. Improvements and application of a streamlined, higher-throughput method for testing solution stability to support drug discovery are described. Mass spectrometry detection has been incorporated into the screen to allow for the identification of degradation products. The amount
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Dissertations / Theses on the topic "Drug solution"

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Wheeler, Daniel Wren. "Weakened by strengths : drugs in solution, medication error and drug safety." Thesis, University of Oxford, 2008. http://ora.ox.ac.uk/objects/uuid:238087a5-120b-4a3d-9437-5840cecf8b6a.

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The concentrations of some drug solutions are often expressed as ratios or percentages. This system simplified prescription and dispensing when Imperial measures such as grains and minims were used. Ampoules of powerful vasoactive drugs such as catecholamines and potentially toxic local anaesthetics are still labelled as ratios and percentages, seemingly through habit or tradition than for any useful clinical reason. This thesis argues that adherence to this outdated system is confusing, causes drug administration errors, and puts patients at risk. Internet-based questionnaires were used to qu
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Ḥamdān, ʿImād. "Free solution capillary electrophoresis in the study of drug DNA interactions." Thesis, University of Strathclyde, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.249881.

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Zhang, Huixian. "Multicomponent diffusion of macromolucule-additive and drug-surfactant aqueous ternary systems." [Fort Worth, Tex.] : Texas Christian University, 2009. http://etd.tcu.edu/etdfiles/available/etd-04292009-164431/unrestricted/Zhang.pdf.

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Ramirez, Carmen Hernandez. "Enhancement of the rate of solution of relatively insoluble drugs from solid-solid systems prepared by supercritical fluid technology." Columbus, Ohio : Ohio State University, 2007. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1179928429.

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Corswant, Christian von. "Lecithin-based microemulsions for pharmaceutical use phase behavior and solution structure /." Lund : Lund University, 1998. http://catalog.hathitrust.org/api/volumes/oclc/68945035.html.

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Craig, Duncan Quinnell Mackenzie. "Characterisation of the solid and solution state properties of drug dispersions in polyethylene glycols." Thesis, University College London (University of London), 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.321274.

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Zhang, Kangling. "Determination of solution structure of anti-cancer drug etoposide by NMR and computer simulation." Scholarly Commons, 1997. https://scholarlycommons.pacific.edu/uop_etds/2323.

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2.9 mM etoposide in CDCl3 and CDCl3/(D20) were studied at 300 and 500 MHz NMR. One dimensional (1D) NMR spectra and truncated lD Nuclear Overhauser Effect (NOE) buildup experiments were used to find direct information on the structure of etoposide. Results showed that the E-ring rotates freely about the C1’-C4 bond and is oriented to the side where H2’, H4 project. The C and D rings have a "trans" junction at C2-C3 bond. The ethylidene-glucopyranosyl group approaches the D ring allowing close interaction between H1” and H8. Water spin - transfer experiments were done to determine the interacti
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Katayama, Derrick S. "Towards a mechanistic understanding of pharmaceutical protein stabilization in solution and the solid state /." Connect to full text via ProQuest. Limited to UCD Anschutz Medical Campus, 2006.

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Thesis (Ph.D. in Pharmaceutical Sciences) -- University of Colorado at Denver and Health Sciences Center, 2006.<br>Typescript. Includes bibliographical references (leaves 159-173). Free to UCDHSC affiliates. Online version available via ProQuest Digital Dissertations;
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Park, Jongryul. "Poly(2-oxazoline) architectures for drug delivery systems." Thesis, Queensland University of Technology, 2021. https://eprints.qut.edu.au/211439/1/Jongryul_Park_Thesis.pdf.

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The overall aim of my PhD research was to develop biocompatible materials, namely poly(2-oxazoline)s, in terms of chemical structures and chemical and physical properties for drug delivery systems. This thesis demonstrated novel strategies and unique approaches towards sophisticated drug delivery formulations. A combination of crosslinking chemistry, thermoresponsive properties, and drug conjugation was introduced to overcome common issues in typical drug delivery devices such as burst drug release and low drug efficiency. Ultimately, this thesis aimed to promote poly(2-oxazoline)s as the most
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Fiebrig, Immo. "Solution studies on the mucoadhesive potential of various polymers for use in gastrointestinal drug delivery systems." Thesis, University of Nottingham, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307747.

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Books on the topic "Drug solution"

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Mitchell, Chet N. The drug solution. Carleton University Press, 1990.

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Mansfield, John. Migraine: The drug-free solution. Thorsons Publishers, 1987.

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National Institute on Drug Abuse, ed. Drug abuse treatment: A community solution. Dept. of Health and Human Services, Public Health Service, Alcohol, Drug Abuse, and Mental Health Administration, National Institute on Drug Abuse, 1989.

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Millar, Cormac. An Irish solution. Penguin Ireland, 2004.

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Bugliosi, Vincent. The phoenix solution: Getting serious about winning America's drug war. Dove Books, 1996.

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Sadler, Jan. A good night's sleep: A drug-free solution. Healing Arts Press, 2008.

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Mansfield, John. Migraine and the allergy connection: A drug-free solution. 2nd ed. Healing Arts Press, 1990.

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Pirilä-Honkanen, Päivi. Physicochemical properties of 2-pyrrolidinone and n-methylbenzenesulfonamide in binary solution mixtures. Oulun Yliopisto, 1996.

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Lanza, Juliana Micai. L'accès aux médicaments au Brésil: Le droit comme source et solution du problème. Éditions Thémis, 2009.

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Guido, Jim. A crack in the wall: The unspeakable solution. Global Heart Books, 1995.

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Book chapters on the topic "Drug solution"

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Peet, Norton P., and Hwa-Ok Kim. "Parallel Solution-Phase Synthesis." In Drug Discovery and Development. John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0471780103.ch5.

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Nishimura, Shin-Ichiro. "Solution and Polymer-Supported Synthesis of Carbohydrates." In Carbohydrate-Based Drug Discovery. Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527602437.ch5.

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McKeganey, Neil. "Drug Legalization: Solution or Social Problem?" In Controversies in Drugs Policy and Practice. Macmillan Education UK, 2011. http://dx.doi.org/10.1007/978-0-230-36518-6_7.

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Thaher, Yasmin, Shehdeh Jodeh, and Othman Hamed. "Extraction of Drug Residuals from an Aqueous Solution Using Nanocellulose Adsorbent." In Recent Advances in Environmental Science from the Euro-Mediterranean and Surrounding Regions (2nd Edition). Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-51210-1_136.

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Tranvåg, Eirik Joakim, and Roger Strand. "Rationing of Personalised Cancer Drugs: Rethinking the Co-production of Evidence and Priority Setting Practices." In Human Perspectives in Health Sciences and Technology. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-92612-0_14.

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AbstractRising health care costs is a challenge for all health care systems, and new and expensive cancer drugs is an important contributor to this. Many countries – like Norway – have therefore established priority setting institutions and systems for drug appraisals where equal treatment, neutrality and transparency are key values. Despite this, controversy surrounding drug reimbursement decisions are persistent.The development of personalised cancer medicine is seen by many as a potential solution to difficult priority setting decisions, by tailoring the right drug to the right patient at t
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Nagy, Peter I. "Theoretical Consideration of In-Solution Tautomeric Equilibria in Relation to Drug Design." In Tautomerism. Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527695713.ch6.

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"Drug Rationing." In The Drug Solution. McGill-Queen's University Press, 1990. http://dx.doi.org/10.1515/9780773595828-010.

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Di, Li, and Edward H. Kerns. "Solution Stability." In Drug-Like Properties. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-12-801076-1.00013-7.

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Di, Li, and Edward H. Kerns. "Solution Stability Methods." In Drug-Like Properties. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-12-801076-1.00031-9.

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"Bimatoprost (ophthalmic solution)." In PharmacotherapyFirst Drug Information. The American Pharmacists Association, 2017. http://dx.doi.org/10.21019/druginformation.bimatoprost_ophthalmic_solution.

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Conference papers on the topic "Drug solution"

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Maram, Sai Pragnya, Durga Vinila Lella, Sukruthi Maddala, Shivani Madupathi, Sanksheet Katikela, and Srinuvasarao Sanapala. "Medication Access Made Easy: A Location-Based Solution for Real-Time Drug Availability." In 2024 5th IEEE Global Conference for Advancement in Technology (GCAT). IEEE, 2024. https://doi.org/10.1109/gcat62922.2024.10923850.

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Monisha, R., Sowmya Ramkumar, and D. Nalini. "Experimental and Density Function Theory Calculations to Investigate the Adsorption of an Anti-inflammatory Drug on Aluminum Surface in Acid Solution." In CORROSION 2016. NACE International, 2016. https://doi.org/10.5006/c2016-07517.

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Abstract The literature dealing with aluminium behavior in acid media in the presence of an anti-inflammatory drug is studied in order to understand its action mechanism, protective film formed and the possibility of its application according to the inhibition efficiency achieved. Aceclofenac, an anti-inflammatory drug is studied and its inhibitive performance on aluminium corrosion was studies by both dry and wet lab studies. Dry lab process using DFT is used to explore the relationship between the inhibitor molecular property and its inhibition efficiency. Wet lab studies have been carried o
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Cao, Xinyu, Yifan Song, Jiayuan Wang, Linyu Zhu, and Xi Chen. "Bayesian Optimization for Enhancing Spherical Crystallization Derived from Emulsions: A Case Study on Ibuprofen." In The 35th European Symposium on Computer Aided Process Engineering. PSE Press, 2025. https://doi.org/10.69997/sct.158833.

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The pharmaceutical industry is a highly specialized field where strict quality control and accelerated time-to-market are essential for maintaining competitive advantage. Spherical crystallization has emerged as a promising approach in pharmaceutical manufacturing, offering significant potential to reduce equipment and operating costs, enhancing drug bioavailability, and facilitating compliance with product quality regulations. Emulsions, as an enabling technology for spherical crystallization, present unique advantages. However, the quality of spherical crystallization products derived from e
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Li, Kun, Weiwei Liu, Yong Luo, Xiantao Cai, Jia Wu, and Wenbin Hu. "Zero-shot Learning for Preclinical Drug Screening." In Thirty-Third International Joint Conference on Artificial Intelligence {IJCAI-24}. International Joint Conferences on Artificial Intelligence Organization, 2024. http://dx.doi.org/10.24963/ijcai.2024/234.

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Conventional deep learning methods typically employ supervised learning for drug response prediction (DRP). This entails dependence on labeled response data from drugs for model training. However, practical applications in the preclinical drug screening phase demand that DRP models predict responses for novel compounds, often with unknown drug responses. This presents a challenge, rendering supervised deep learning methods unsuitable for such scenarios. In this paper, we propose a zero-shot learning solution for the DRP task in preclinical drug screening. Specifically, we propose a Multi-branc
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Kaneko, Toshiro, Kei Kikuchi, Shota Sasaki, and Makoto Kanzaki. "Plasma-irradiated solution as drug permeation enhancer." In 2016 IEEE International Conference on Plasma Science (ICOPS). IEEE, 2016. http://dx.doi.org/10.1109/plasma.2016.7534290.

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Gupta, Karan, Nitin Rakesh, Neetu Faujdar, Madhuri Kumari, Pawan Kinger, and Rakesh Matam. "IOT Based Automation and Solution for Medical Drug Storage: Smart Drug Store." In 2018 8th International Conference on Cloud Computing, Data Science & Engineering (Confluence). IEEE, 2018. http://dx.doi.org/10.1109/confluence.2018.8443023.

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Dugar, Sundeep. "Introducing LADR4 - A Platform Technology Solution to Make Drug Repurposing a Viable Solution." In RExPO23. REPO4EU, 2023. http://dx.doi.org/10.14293/s2199-1006.1.sor-.ppwa3eq.v1.

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Dugar, Sundeep. "Introducing LADR4 - A Platform Technology Solution to Make Drug Repurposing a Viable Solution." In RExPO23. REPO4EU, 2023. http://dx.doi.org/10.58647/rexpo.23000013.v1.

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Bavali, A., P. Parvin, and R. Karimi. "Blue Spectral Shift of Laser-Induced Fluorescence Due to Suspension of Nano-structures in Rd6G Solution." In Optical Molecular Probes, Imaging and Drug Delivery. OSA, 2015. http://dx.doi.org/10.1364/omp.2015.om4d.2.

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Rautiola, Davin, and Ronald A. Siegel. "Nasal Spray Device for Administration of Two-Part Drug Formulations." In 2019 Design of Medical Devices Conference. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/dmd2019-3216.

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Intranasal drug delivery is an attractive route to noninvasively achieve a rapid therapeutic effect, avoid first pass metabolism, and bypass the blood brain barrier. However, the types of drugs that can be administered by this route has been limited, in part, by device technology. Herein, we describe a pneumatic nasal spray device that is capable of mixing liquid and solid components of a drug formulation as part of the actuation process during dose administration. The ability to store a nasal spray drug formulation as two separate components can be leveraged to solve a variety of stability is
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Reports on the topic "Drug solution"

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Rujiravanit, Ratana. Preparation and characterization of hydrogel from chitin derivative and silk fibroin. Thailand Research Fund, 2003. https://doi.org/10.58837/chula.res.2003.80.

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Natural polymer blend films composed of chitosan and silk fibroin were prepared by solution casting technique with various ratios of chitosan to silk fibroin, using glutaraldehyde as crosslinking agent. The effects of the ratio of chitosan to silk fibroin and crosslinking agent on mechanical properties, swelling behavior and drug releasing property of the blend films were studied. For the swelling behavior, the blend films exhibited a dramatic change in the degree of swelling when immersed in acidic solutions. The blend film with 80% chitosan content had the maximum degree of swelling. It appe
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Zhang, Cheng, and Yue Yang. Impact of adaptive design on reducing the duration of clinical trials in rare cancers: a meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.2.0081.

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Review question / Objective: Whether the application of adaptive design in clinical trials of rare cancers can shorten the duration of clinical trials? Condition being studied: Currently, the development of innovative drug products (InMPs) for rare cancers faces many challenges, including the difficulty of enrolling sufficient numbers of patients from small and heterogeneous patient populations for clinical trials, and the significant risks of high financial investment, long development times and potential failure from a pharmaceutical company's perspective for rare cancer drugs due to limited
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Conteh, Abu. SSHAP West Africa Hub: Addressing the Kush Epidemic in Sierra Leone. Institute of Development Studies, 2024. http://dx.doi.org/10.19088/sshap.2024.060.

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Sierra Leone has seen a sharp rise in the use of ‘kush’ – a relatively new drug formed through mixing several constituent drugs, including opioids, which is proving highly addictive and is having serious negative health and social consequences. In April 2024, the government declared a public health emergency resulting from high levels of kush use, with security services launching crackdowns.1 Limited data on kush use presents challenges to understanding the scale of the problem. The lack of evidence has hampered the government’s response to the kush crisis. This has contributed to a misunderst
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Hershberg, Elliot, and Nicholas McCarty. Beyond Steel Tanks. Asimov Press, 2024. http://dx.doi.org/10.62211/72po-11rs.

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Segletes, Steven B., and William P. Walters. Analytical Solution in Curvilinear Coordinates for the Trajectory of a Projectile Subject to Aerodynamic Drag. Defense Technical Information Center, 2011. http://dx.doi.org/10.21236/ada553963.

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Zheng, Wanzheng, and Jason Merret. Aerodynamic Survey of Novel eVTOL Configuration Using SU2. Illinois Center for Transportation, 2022. http://dx.doi.org/10.36501/0197-9191/22-014.

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This report summarizes computational fluid dynamics (CFD) results of electric vertical takeoff and landing (eVTOL) geometries using the SU2 Reynolds-averaged Navier-Stokes (RANS) solver. Geometries were generated based on the Smart Transportation Infrastructure Initiative (STII) Rappor 15th iteration with various rotor-installment solutions. It was found that although open rotors installed on an underwing pylon were superior to shrouded rotors installed in a canoe, the canoe configuration would provide more potential for improvement, and using a canoe door to cover the first rotor opening woul
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Tengamnuay, Parkpoom. Efficacy and mechanistic studies of chitosan as nasal absorption enhancer of peptide drugs : research report. Chulalongkorn University, 1999. https://doi.org/10.58837/chula.res.1999.27.

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Objective. To evaluation the in vivo efficacy of chitosan as nasal absorption enhancers of peptides in rats and compare the results with that of hydroxypropyl- and dimethyl-Beta-cyclodextrins (HPBetaCD and DMBetaCD). Methods. Two types of chitosan. i.e., the free base (CSJ) and the glutamate salt form (CSG) were evaluated for their nasal absorption enhancing effect on salmon calcitonin (sCT) using an in vibo rat absorption technique. Solutions containing sCT and chitosan (0 to 1.25 % w/v) in isotonic phosphate buffers (pH 3.0 to 6.0) were nasally administered at the dose of 10 IU/kg. The plasm
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Sudhivoraseth, Jitraporn. Policy evaluation on promotion projects implemented by the Public Relations Department's Regional Offices. National Institute of Development Administration ; Chulalongkorn University, 2002. https://doi.org/10.58837/chula.res.2002.21.

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This research aims to study the achievement or failure of the promotion projects implemented by the Public Relations Department’s Regional Offices. The objectives of this study are two fold. First, to evaluate the three promotion projects: Democracy Promotion Project, Drug Prevention and Solution Promotion Project, and AIDS Prevention and Solution Promotion Project under the Action Plan of the Public Relations Department, fiscal year 2000. Second, to investigate the factors relating to the achievements or failures of these three promotion projects under study. The conceptual framework is devel
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Pasupuleti, Murali Krishna. AI and Quantum-Nano Frontiers: Innovations in Health, Sustainability, Energy, and Security. National Education Services, 2025. https://doi.org/10.62311/nesx/rr525.

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Abstract: This research report explores transformative advancements at the intersection of Artificial Intelligence (AI), Quantum Computing, and Nanotechnology, focusing on breakthrough innovations in health, sustainability, energy, and global security. By integrating quantum algorithms, AI-driven analytics, and advanced nanomaterials, this report highlights revolutionary solutions in precision medicine, predictive diagnostics, sustainable energy storage, universal water purification, and cybersecurity. Real-world case studies and emerging technologies such as graphene-based nanomaterials, quan
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10

Banerjee, Pritam, and Atul Sanganeria. Developing a Risk Management System for Participating Government Agencies of India. Asian Development Bank, 2021. http://dx.doi.org/10.22617/wps210413-2.

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Trade facilitation is a critical building block of developing globally integrated value chains. In India, current trade facilitation systems including risk assessment criteria require improvements involving regulatory mandates for food and drugs, animal and plant quarantine, wildlife protection, and textile products. Using illustrative examples, this working paper presents specific system development needs for six major participating government agencies on trade facilitation in India. It provides a model for developing a comprehensive system of risk management. It also discusses the need for i
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