Potassium dihydrogen phosphate 3.402% / Potassium hydroxide 0.28% (total potassium 30mmol/100ml) / Disodium phosphate dihydrate 2.67g infusion 100ml bags
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View all licensed products for Potassium dihydrogen phosphate + Potassium hydroxide + Disodium phosphate dihydrate on the MHRA register
Potassium dihydrogen phosphate 3.402% / Potassium hydroxide 0.28% (total potassium 30mmol/100ml) / Disodium phosphate dihydrate 2.67g infusion 100ml bags
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
1945–2026
Showing the 50 most relevant studies, sorted by most relevant.
Frits Zernike
Journal of the Optical Society of America, 1964
J. Jerphagnon, S. K. Kurtz
Physical Review B, 1970
W. P. Mason
Physical Review, 1946
M. Kumar, J. Xie, K. Chittur, et al.
Biomaterials, 1999
D. Singh, K. N. Hareendran, T. Sreenivas, et al.
Hydrometallurgy, 2017
F. Y. Wu
Physical Review, 1968
P. S. Peercy
Physical Review Letters, 1973
L. B. Harris, G. J. Vella
The Journal of Chemical Physics, 1973
Kristina Jančaitienė, Rasa Šlinkšienė, Renata Žvirdauskienė
Open Agriculture, 2023
Abstract One of the challenges of the modern world is to improve human nutrition and to safely increase the yield of agricultural production using existing agricultural land. It is clear that sufficient agricultural efficiency cannot be achieved without fertilizers, but fertilizers must cause minimal damage to the soil. Microorganisms, such as spore-forming bacteria, actinomycetes, fungi, algae, and protozoa play an important role in the soil and keep soil healthy. One of the soil substances involved in reactions that take place in plants is cellulose. This study investigated the effect of potassium dihydrogen phosphate (PDP), synthesized (via conversion between potassium chloride and ammonium dihydrophosphate) and granulated with the addition of microcrystalline cellulose (MC), on plants (winter wheat Toras, Lithuania) and soil microorganisms. The data of plants fertilized with pure KH2PO4, ones fertilized with PDP granulated with MC, and grown without fertilizers were compared in this study. Scanning electron microscopy and differential scanning calorimetry analysis were used to characterize the obtained product. One-way analysis of variance was used to evaluate the differences of the mean values between groups. In all cases, the significance level was p ≤ 0.05. The effect of pure KH2PO4 on plant indicators was found to be lower than that of granular PDP with MC. The length of the leaves was 29.63 and 31.20 cm, green mass was 0.471 and 0.763 g, ash mass was 0.015 and 0.019 g, respectively. In addition, granular PDP with MC did not adversely affect the soil microorganisms because the number of any species of bacteria (Spore b., mineral nitrogen assimilating bacteria, cellulose degrading bacteria) did not decrease and a slight increase in the number of Actinomycetes (from 8.5 × 105 to 2.9 × 106 KSV/g) and molds (from 3.0 × 104 to 1.4 × 105 KSV/g) was observed. The granular PDP with MC that we developed and used have better physical properties, higher agrochemical efficiency and cause less harm to soil microorganisms compared to pure PDP.
Abstract licence: CC BY 4.0
Eggers DK, Le JM, Nham NT, et al.
2024
This study examines the role of water in binding equilibria with a special focus on secondary solutes (cosolutes) that influence the equilibrium but are not constituents of the final product. Using a thermodynamic framework that includes an explicit term for the release of water molecules upon binding, this investigation reveals how solutes may alter equilibria by changing the activity of the reactants, reflected in ΔG°(obs), and by changing the chemical potential of the solvent, reflected in ΔGS. The framework is applied to four experimental binding systems that differ in the degree of electrostatic contributions. The model systems include the chelation of Ca2+ by EDTA and three host-guest reactions; the pairings of p-sulfonatocalix[4]arene with tetramethylammonium ion, cucurbit[7]uril with N-acetyl-phenylalanine-amide, and β-cyclodextrin with adamantane carboxylate are tested. Each reaction pair is examined by isothermal titration calorimetry at 25 °C in the presence of a common osmolyte, sucrose, and a common chaotrope, urea. Molar solutions of trehalose and phosphate were also tested with selected models. In general, cosolutes that enhance binding tend to reduce the solvation free energy penalty and cosolutes that weaken binding tend to increase the solvation free energy penalty. Notably, the nonpolar-nonpolar interaction between adamantane carboxylate and β-cyclodextrin is characterized by a ΔGS value near zero. The results with β-cyclodextrin, in particular, prompt further discussions of the hydrophobic effect and the biocompatible properties of trehalose. Other investigators are encouraged to test and refine the approach taken here to further our understanding of solvent effects on molecular recognition.
Abstract licence: CC BY-NC-ND
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.