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1.
PLoS One ; 16(5): e0251808, 2021.
Article in English | MEDLINE | ID: mdl-33999939

ABSTRACT

OBJECTIVES: To compare blood alkalosis, gastrointestinal symptoms and indicators of strong ion difference after ingestion of 500 mg.kg-1 BM sodium citrate over four different periods. METHODS: Sixteen healthy and active participants ingested 500 mg.kg-1 BM sodium citrate in gelatine capsules over a 15, 30, 45 or 60 min period using a randomized cross-over experimental design. Gastrointestinal symptoms questionnaires and venous blood samples were collected before ingestion, immediately post-ingestion, and every 30 min for 480 min post-ingestion. Blood samples were analysed for blood pH, [HCO3-], [Na+], [Cl-] and plasma [citrate]. Linear mixed models were used to estimate the effect of the ingestion protocols. RESULTS: For all treatments, blood [HCO3-] was significantly elevated above baseline for the entire 480 min post-ingestion period, and peak occurred 180 min post-ingestion. Blood [HCO3-] and pH were significantly elevated above baseline and not significantly below the peak between 150-270 min post-ingestion. Furthermore, blood pH and [HCO3-] were significantly lower for the 60 min ingestion period when compared to the other treatments. Gastrointestinal symptoms were minor for all treatments; the mean total session symptoms ratings (all times summed together) were between 9.8 and 11.6 from a maximum possible rating of 720. CONCLUSION: Based on the findings of this investigation, sodium citrate should be ingested over a period of less than 60 min (15, 30 or 45 min), and completed 150-270 min before exercise.


Subject(s)
Bicarbonates/blood , Exercise , Sodium Citrate , Adult , Alkalosis , Female , Gastrointestinal Diseases , Humans , Male , Sodium Citrate/administration & dosage , Sodium Citrate/pharmacokinetics
2.
Biol Pharm Bull ; 44(2): 266-270, 2021.
Article in English | MEDLINE | ID: mdl-33518679

ABSTRACT

Extracellular pH (pHe) of tumor cells is characteristic of tumor microenvironment (TME). Acidic TME impairs the responses of tumors to some anti-cancer chemotherapies. In this study, we showed that daily oral dosing of sodium potassium citrate (K/Na citrate) increased blood HCO3- concentrations, corresponding to increase of HCO3- concentrations and pHs in urine, and neutralized the tumor pHe. Neutralization of acidic TME by alkaline substance like HCO3-, an active metabolite of K/Na citrate, well potentiated the therapeutic effect of anticancer agent TS-1®, an orally active 5-fuluoro-uracil derivative, in Panc-1 pancreatic cancer-xenograft murine model. Neutralization of acidic TME by using an alkaline K/Na citrate is a smart approach for enhancement of the therapeutic effects of anticancer agents for pancreatic cancer in the end stage.


Subject(s)
Antacids/administration & dosage , Hydrogen-Ion Concentration/drug effects , Oxonic Acid/administration & dosage , Pancreatic Neoplasms/drug therapy , Tegafur/administration & dosage , Tumor Microenvironment/drug effects , Administration, Oral , Animals , Antacids/pharmacokinetics , Cell Line, Tumor , Drug Combinations , Drug Synergism , Extracellular Space/chemistry , Extracellular Space/drug effects , Female , Humans , Mice , Oxonic Acid/pharmacokinetics , Oxonic Acid/therapeutic use , Pancreatic Neoplasms/pathology , Potassium Citrate/administration & dosage , Potassium Citrate/pharmacokinetics , Sodium Citrate/administration & dosage , Sodium Citrate/pharmacokinetics , Tegafur/pharmacokinetics , Tegafur/therapeutic use , Xenograft Model Antitumor Assays
3.
ACS Appl Mater Interfaces ; 11(29): 25730-25739, 2019 Jul 24.
Article in English | MEDLINE | ID: mdl-31299144

ABSTRACT

Enhancement of permeability and the retention effect is one of the main pathways for the accumulation of nanomaterials in tumor sites, but poor cellular internalization and rapid clearance of nanomaterials always hamper the efficacy of imaging diagnosis and treatment. With the consideration of both high tumor accumulation and cellular internalization, positively charged nanomaterials can adhere to the tumor cell membrane by an electrostatic force, which is conducive to cellular internalization, but they are easily recognized and cleared during blood circulation. However, negatively charged nanomaterials show an enhanced stealth-like effect and possess a long blood circulation time, which is conducive to tumor accumulation. Therefore, in this work, on the basis of the shielding effect of citrate ions to positive charge and the protonation under an acidic tumor microenvironment, pH-sensitive sodium citrate-modified polyaniline nanoshuttles (NSs) with negative charge during blood circulation but positive charge in tumor sites are designed. With this hierarchical targeting strategy, the blood circulation half-life increases from 4.35 to 7.33 h, and the retention rate of NSs in tumors increases from 5.29 to 8.57% ID/g. Because the retention rate of NSs is increased, the magnetic resonance imaging resolution and signal intensity are significantly improved. A synergistic treatment of tumors is further achieved by means of photothermal therapy with laser irradiation and chemotherapy via heat-stimulated drug release.


Subject(s)
Drug Carriers , Nanostructures , Neoplasms, Experimental , Sodium Citrate , Theranostic Nanomedicine , Tumor Microenvironment/drug effects , Aniline Compounds , Animals , Cell Line, Tumor , Drug Carriers/chemistry , Drug Carriers/pharmacokinetics , Drug Carriers/pharmacology , Humans , Mice , Mice, Nude , Nanostructures/chemistry , Nanostructures/therapeutic use , Neoplasms, Experimental/drug therapy , Neoplasms, Experimental/metabolism , Neoplasms, Experimental/pathology , Sodium Citrate/chemistry , Sodium Citrate/pharmacokinetics , Sodium Citrate/pharmacology
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