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DOI: 10.3329/icpj.v1i1.9219
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Arsenic, the poison and poisoned groundwater of Bangladesh: A review

Abstract: DOI: http://dx.doi.org/10.3329/icpj.v1i1.9219 International Current Pharmaceutical Journal 2011, 1(1): 12-17

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Cited by 16 publications
(14 citation statements)
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“…Like arsenic, awareness can be increased through the government and non government program by using electronic media, mass media, print media etc. (Uddin et al, 2011).…”
Section: Awareness Of the Respondents About The Appropriate Healthcarmentioning
confidence: 99%
“…Like arsenic, awareness can be increased through the government and non government program by using electronic media, mass media, print media etc. (Uddin et al, 2011).…”
Section: Awareness Of the Respondents About The Appropriate Healthcarmentioning
confidence: 99%
“…There are an increasing number of complex active pharmaceutical ingredients (APIs) being developed which fall into the biopharmaceutical classification system (BCS) classes II/IV and, hence, have poor solubility in the gastrointestinal (GI) tract exhibiting slow dissolution rate behavior with concomitantly low bioavailability. The design of poorly soluble drug compounds to overcome these issues with bioavailability remains a persistent challenge due to an insufficient understanding of the optimal dissolution characteristics from first principles. Dissolution is also an important process in the wider chemical industry, such as the nuclear industry, and similar areas such as physics, biology, and environmental science. , Dissolution and crystal growth can be considered to be a series combination of mass transfer (diffusion down a concentration gradient away from/toward the crystal surface into/from the bulk solution) and crystal interfacial kinetics (the mechanism by which a molecule detaches or attaches itself from/to a crystal surface). , However, current dissolution models are still based on the Noyes-Whitney equation: normald m normald t = D δ A ( c * c ) where the change in mass over time (d m /d t , kg s –1 ) is described by the diffusion coefficient ( D , m 2 s –1 ), boundary layer (BL) thickness (δ, m), surface area ( A , m 2 ), and the difference in the equilibrium solution concentration and the solute concentration in the bulk solution ( c * – c , kg m –3 ). This model is based on bulk properties of the crystal and assumes diffusional processes govern dissolution.…”
Section: Introductionmentioning
confidence: 99%
“…This linker, which increased the peptide-dye distance,w as introduced to avoid overlap of the dye with the receptor-recognizing pharmacophore of the peptidec arrier. [27] The obtained OCTA-G-XCy conjugate was then coupled to the anticancer drug CLB to form an ovel TDD system,O CTA-G-XCy-CLB,t hat was demonstrated to enable fluorescence monitoring of drug release within the NIR spectral region.C LB was bound to XCy by meanso fahydrolytically cleavable ester bond, which is knownt ob ep redominantly hydrolyzedi n tumors under physiological conditions in the presence of esterases. [28] At the same time, the ester linker is provent ob e stable enoughi nt he bloodstream for targeted delivery of these agents to cancer tissue, and therefore, it is used for the conjugation of variousa nticancer agents, such as camptothecin and doxorubicin.…”
Section: Introductionmentioning
confidence: 99%