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Calcium, Dietary

Calcium, Dietary refers to the intake of calcium-containing foods and supplements as part of the diet.
Dietary calcium is essential for maintaining healthy bones, teeth, and overall body function.
It plays a crucial role in processes like muscle contraction, nerve function, and blood clotting.
Sufficient calcium intake can help prevent osteoporosis and reduce the risk of fractures, particularly in older adults.
Sources of dietary calcium include dairy products, leafy greens, fortified foods, and calcium supplements.
Maintaining the appropriate dietary calcium balance is important for optimizing bone health and preventing calcium-related disorders.
Researchers can leverge PubCompare.ai's AI-powered platform to optimize their dietary calcium research protocols, locating the best procedures from literature, pre-prints, and patents through efficient comparisons to improve reproducibility and accuracy in this critical area of nutrition and health.

Most cited protocols related to «Calcium, Dietary»

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Publication 2010
Bath Calcium, Dietary HEPES propylene Sodium Azide Zinc
We used a semi-quantitative FFQ of 101 food items to assess the usual daily intake of foods and nutrients (available at: http://bibliodieta.umh.es/files/2011/07/CFA101.pdf). The FFQ was a modified version from a previous FFQ based on the Harvard questionnaire [15 (link)], which we developed and validated using four 1-week dietary records in an adult population in Valencia. The validity correlation coefficients (adjusted for energy intake) ranged from 0.27 for folate intake to 0.67 for calcium intake (average 0.47), and the reproducibility correlation coefficient s ranged from 0.30 for carotene intake to 0.65 for calcium intake (average 0.40) [16 ,17 (link)]; this is a similar range to other established diet questionnaires [3 ,4 (link)]. For the dietary assessment of pregnant women in the INMA cohort study, we added additional food items in the FFQ in order to capture the major sources of the most relevant nutrients, including specific carotenoids.
Participants in the study were asked twice during pregnancy how often, on average, they had consumed each food item over two periods of several months. The first period covered the time from the last menstruation to the first prenatal visit that occurred between the 10–13 weeks of pregnancy; the second period was the time between the first visit and the second one between weeks 28–32 of gestation. Serving sizes were specified for each food item in the FFQ. The questionnaire had nine possible responses, ranging from ‘never or less than once per month’ to ‘six or more per day’. Additionally, we asked whether study participants followed special diets.
Nutrient values were primarily obtained from the food composition tables of the US Department of Agriculture publications as well as other published sources for Spanish foods and portion sizes [18 ,19 ]. In order to obtain average daily nutrient intakes from diet for each individual, we multiplied the frequency of use for each food by the nutrient composition of the portion/serving size specified on the FFQ and added the results across all foods. For those nutrients often used in supplements during pregnancy such as folate, vitamin C and vitamin B12, the total daily nutrient intake was estimated by adding the average daily intake from supplements and the usual daily nutrient intake from the FFQ. In order to convert folic acid intake from supplements to dietary folate, we used the equivalence of 1 mcg of folate in the diet equals to 0.6 mcg of folic acid from supplements [20 (link)]. We estimated the mean daily consumption for 17 foods and food groups by grouping the intake of specific foods in the FFQ (Table 1).
Publication 2013
A-101 Adult Ascorbic Acid Calcium, Dietary Carotene Carotenoids Cobalamins Diet Dietary Supplements Eating Folate Folic Acid Food Hispanic or Latino Menstruation Nutrient Intake Nutrients Pregnancy Pregnant Women
GCaMPs in pRSETa were transformed into chemically competent BL21(DE3)-pLysS, and purified via the N-terminal His tag. Protein concentration was determined by intrinsic tryptophan fluorescence. Calcium clamping was performed at pH 7.2 with 10 mM blends of K2H2EGTA and Ca2EGTA from the Calcium Calibration Kit #1 (Invitrogen). Free [Ca2+] levels were calculated using MAXCHELATOR (maxchelator.stanford.edu). Fluorescence spectra were recorded on a Safire2 (link) fluorescence plate reader (Tecan). The dynamic range here is calculated as Fmax/Fmin. Fmax is the fluorescence intensity at saturating [Ca 2+] and Fmin is the fluorescence intensity at zero [Ca 2+].
Publication 2009
Calcium, Dietary Fluorescence Proteins Tryptophan
Alginate probes were prepared using extrusion methods [18 (link)], [19 (link)]. Briefly, 1% sodium alginate in water functioned as the anionic solution and 2% calcium chloride containing 1% carboxymethylcellulose functioned as the cationic solution. Functionalized mNPs [12 ] (Micromod, 100 nm hydrodynamic diameter, iron oxide, dextran coated) were added to the cationic solution to achieve 1 mg/ml concentration. Droplets of the cationic solution were injected into 100 ml of anionic solution under constant stirring to generate hollow core beads. After alginate beads formed, they were rinsed with 2% calcium chloride three times, and incubated in 0.01% calcium solution at 4 °C. The resulting probes proved stable for two months. For spectroscopic measurements, calcium-alginated beads containing around 300 μg mNP were used.
We used blood as a surrogate for the interstitial in vivo environment. Blood contains most of the chemical complexities of the in vivo environment: the antibodies, enzymes, and a host of other proteins large and small present in vivo are all present in blood. Other biological samples are generally less problematic: urea, saliva, tissue, and so on. Blood is also the most commonly collected biological sample and has the most complicated composition. It has been shown that mNPs were readily taken in by cells resulting in a lower MSB signal [11 ]. Whole blood was harvested in an eppendorf tube containing heparin from the vena cava of euthanized C57BL/6 mice using a 3 mL syringe and a 25G needle. The whole blood was spun at 4500 r/min for 20 min at 4 °C, and the supernatant was used for experiments as plasma.
The spectroscopic measurements for the probe data were acquired at 1270 Hz on our original apparatus [9 ]–[12 ]. The ratio of the fifth over the third harmonics of the mNP magnetization was used as a concentration-independent metric [9 ], [10 (link)].
In the second arm of this paper, we tested the sensitivity of a recently introduced spectrometer that measures the magnetization perpendicular to the oscillating applied field. The perpendicular magnetization is induced by applying a small static field perpendicular to the oscillating applied field [20 (link)].
Publication 2015
Alginate Antibodies Biopharmaceuticals BLOOD Blood Substitutes Calcium, Dietary Calcium chloride Carboxymethylcellulose Cations Cells Dextran Enzymes ferric oxide Heparin Hydrodynamics Hypersensitivity Mice, Inbred C57BL Needles Plasma Saliva Sodium Alginate Spectrum Analysis Staphylococcal Protein A Syringes Tissues Urea Venae Cavae
We recruited pregnant women from 2001 through 2003 at the Mexican Social Security Institute (Instituto Mexicano del Seguro Social) pre-natal clinics that serve a low- to moderate-income population in Mexico City. We assessed 3,836 women for eligibility, of whom 1,981 did not meet study eligibility criteria (pregnancy of no more than 14 weeks’ gestation; not presenting with a high-risk pregnancy; plans to reside in the metropolitan Mexico City area for ~ 5 years) or had other reasons not being enrolled (n = 2). Of the remaining 1,853 eligible women, 670 (36%) agreed to participate and signed the informed consent, and were randomly assigned to receive a daily supplement of 1,200 mg calcium [two 600-mg calcium carbonate tablets (Wyeth Consumer Health Care/Lederle Laboratories, Inc., México City, México) at bedtime; n = 334] or placebo (n = 336). We assessed blood lead levels, dietary calcium intake, and reported use of lead-glazed ceramics (LGC) at three time points: baseline (first trimester), 6 months (second trimester), and 8 months (third trimester). We assessed compliance by pill count at each follow-up visit. We defined women who had at least one blood lead measurement at 6 or 8 months’ gestation (n = 565; 84%) as having completed follow-up. Eight women did not have baseline blood lead levels, yielding a total of 557 subjects (83%) available for inclusion in the final analyses (Figure 1).
The research protocol was approved by the Human Subjects Committee of the National Institutes of Public Health, the Mexican Social Security Institute, the Brigham and Women’s Hospital, and the Harvard School of Public Health and complied with both Mexican and U.S. federal guidelines governing the use of human participants. All participating mothers received a detailed explanation of the study intent and procedures and were advised on identifying and avoiding LGC pottery use during pregnancy before signing the approved written informed consent.
Publication 2008
BLOOD Calcium, Dietary Carbonate, Calcium Contraceptives, Oral Dietary Supplements Eligibility Determination High-Risk Pregnancy Homo sapiens Infantile Neuroaxonal Dystrophy Mothers Placebos Pregnancy Pregnant Women Woman

Most recents protocols related to «Calcium, Dietary»

Not available on PMC !

Example 10

Compound I Form F was obtained via slurry of Compound I calcium salt hydrate Form A in MEK at room temperature.

A. X-Ray Powder Diffraction

XRPD was performed with a Panalytical X'Pert3 Powder XRPD on a Si zero-background holder. The 20 position was calibrated against a Panalytical Si reference standard disc. The XRPD diffractogram for Compound I Form F is shown in FIG. 16 and summarized in Table 21.

TABLE 21
XRPD signals for crystalline Compound I Form F
Angle (degrees
XRPD Peaks2-Theta ± 0.2)Intensity %
19.14100.0
29.0689.3
35.348.5
47.548.2
510.623.7
611.918.5

Compound I Form F is characterized by the following elemental analysis Table:

CompoundCompound
Batch #CaI:Ca ratioNaI:Na ratio
114%1:25%1:1  
2 7%1:13%1:0.8

Patent 2024
14-3-3 Proteins Calcium, Dietary Powder Salts X-Ray Diffraction

Example 14

Compound I calcium salt EtOH solvate Form C was obtained via slurry of Compound I calcium salt amorphous form in EtOH/H2O (9:1, v:v) at room temperature.

A. X-Ray Powder Diffraction

XRPD on Compound I calcium salt EtOH solvate Form C was performed with a Panalytical X'Pert3 Powder XRPD on a Si zero-background holder. The 2 theta position was calibrated against a Panalytical Si reference standard disc. The XRPD diffractogram for Compound I calcium salt EtOH solvate Form C is shown in FIG. 20 and summarized in Table 25.

TABLE 25
XRPD signals for Compound I calcium
salt EtOH solvate Form C
XRPD Angle (degrees Intensity
Peaks2-Theta ± 0.2)%
14.2100.0
25.043.2
35.713.5

Patent 2024
Calcium, Dietary Ethanol Powder Roentgen Rays Salts

Example 24

Compound I calcium salt cyclopentyl methyl ether (CPME) solvate Form A was obtained via slurry of Compound I calcium salt Form A in IPA/CPME (1:1, v/v) at room temperature.

A. X-Ray Powder Diffraction

XRPD was performed with a Panalytical X'Pert3 Powder XRPD on a Si zero-background holder. The 20 position was calibrated against a Panalytical Si reference standard disc. The XRPD diffractogram for Compound I calcium salt CPME solvate Form A is shown in FIG. 33 and summarized in Table 41.

TABLE 41
Compound I calcium salt
CPME solvate Form A
Angle (degrees
XRPD Peaks2-Theta ± 0.2)Intensity %
15.5100
216.64.38
311.03.86

Patent 2024
Calcium, Dietary Ethyl Ether Powder Salts Sodium Chloride, Dietary X-Ray Diffraction

Example 23

Compound I calcium salt 1,2-dimethoxyethane solvate Form B was obtained via slurry of Compound I calcium salt hydrate Form A in 1,2-dimethoxyethane at room temperature.

A. X-Ray Powder Diffraction

XRPD was performed with a Panalytical X'Pert3 Powder XRPD on a Si zero-background holder. The 20 position was calibrated against a Panalytical Si reference standard disc. The XRPD diffractogram for Compound I calcium salt 1,2-dimethoxy ethane solvate Form B is shown in FIG. 32 and summarized in Table 40.

TABLE 40
Compound I calcium salt
1,2-dimethoxyethane solvate Form B
Angle (degrees
XRPD Peaks2-Theta ± 0.2)Intensity %
14.6100.0
27.743.7
39.130.4
413.727.4
512.123.7
622.920.6
710.119.2
816.518.0
917.014.4
1021.913.6
1119.911.8
1220.711.6
1315.110.7
1423.810.4

Patent 2024
1,2-dimethoxyethane Calcium, Dietary Ethane Powder Salts Sodium Chloride, Dietary X-Ray Diffraction

Example 11

Compound I calcium salt hydrate Form G was obtained via fast cooling of Compound I calcium salt hydrate Form A solution in EtOH:H2O (v:v, 90:10).

A. X-Ray Powder Diffraction:

XRPD was performed with a Panalytical X'Pert3 Powder XRPD on a Si zero-background holder. The 2 theta position was calibrated against a Panalytical Si reference standard disc. The XRPD diffractogram for Compound I calcium salt hydrate Form G is shown in FIG. 17 and summarized in Table 22.

TABLE 22
XRPD signals for crystalline Compound I
calcium salt hydrate Form G
XRPD Angle (degrees Intensity
Peaks2-Theta ± 0.2)%
15.9100.0
214.867.3
314.763.9
46.058.4
58.817.4
611.814.6
711.98.8
826.66.5

Patent 2024
14-3-3 Proteins Calcium, Dietary Ethanol Powder Salts X-Ray Diffraction

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Fluo-4 AM is a fluorescent calcium indicator used for the detection and measurement of intracellular calcium levels. It functions by binding to calcium ions, which results in an increase in fluorescence intensity. This product is commonly used in various cell-based assays and research applications involving calcium signaling.
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Alizarin Red S is a chemical compound used as a dye and a stain in laboratory procedures. It is a red-orange powder that is soluble in water and alcohol. Alizarin Red S is commonly used to stain calcium deposits in histological samples, such as bone and cartilage.
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Fura-2 AM is a fluorescent calcium indicator used for measuring intracellular calcium levels. It is a cell-permeable derivative of the parent compound Fura-2. Fura-2 AM can be loaded into cells, where intracellular esterases cleave off the acetoxymethyl (AM) ester group, trapping the Fura-2 indicator inside the cell.
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HBSS (Hank's Balanced Salt Solution) is a salt-based buffer solution commonly used in cell culture and biological research applications. It provides a balanced ionic environment to maintain the pH and osmotic pressure of cell cultures. The solution contains various inorganic salts, including calcium, magnesium, and potassium, as well as glucose, to support cell viability and homeostasis.
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More about "Calcium, Dietary"

Calcium intake, dietary calcium, calcium-rich foods, calcium supplementation, bone health, osteoporosis prevention, muscle function, nerve signaling, blood clotting, dairy products, leafy greens, fortified foods, calcium balance, Fluo-4 AM, FBS, Alizarin Red S, Fura-2 AM, Penicillin/streptomycin, Bovine serum albumin, DMSO, HBSS, Cetylpyridinium chloride, ADVIA 1800.
Maintaining adequate dietary calcium is essential for overall health and well-being.
Calcium plays a crucial role in a variety of physiological processes, including muscle contraction, nerve function, and blood clotting.
Sufficient calcium intake can help prevent osteoporosis and reduce the risk of fractures, particularly in older adults.
Dietary sources of calcium include dairy products, leafy greens, and fortified foods, while calcium supplements can also be used to meet calcium requirements.
Researchers can leverage PubCompare.ai's AI-powered platform to optimize their dietary calcium research protocols, locating the best procedures from literature, pre-prints, and patents through efficient comparisons to improve reproducibility and accuracy in this critical area of nutrition and health.
Tools like Fluo-4 AM, Fura-2 AM, and ADVIA 1800 can be used to measure and analyze calcium levels in various biological samples.
By maintaining the appropriate dietary calcium balance and utilizing the latest research methods, individuals can optimize their bone health and prevent calcium-related disorders.