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Propylene Glycol

Propylene Glycol is a widely used chemical compound with diverse applications in various industries, including pharmaceuticals, cosmetics, and food production.
It is a clear, colorless, and odorless liquid that serves as a solvent, humectant, and antifreeze agent.
Propylene Glycol is commonly found in a variety of products, such as e-cigarette liquids, lotions, and certain medications.
Researchers and scientists often investigate the efficacy and safety of Propylene Glycol in different applications, focusing on its potential benefits and any possible side effects.
This MeSH term provides a comprehensive overview of Propylene Glycol, its properties, and its diverse uses, aiding in the optimzation of research protocols and enhancing reproducibility.

Most cited protocols related to «Propylene Glycol»

Data were obtained from 9139 subjects [4928 females aged 5–96 years (M = 31.8, SD = 18.9) and 4211 males aged 5–91 years (M = 30.7, SD = 17.7)]. Among them, 3432 (37.5%) had been included in a previous study to establish normative data [15 (link)]. According to the inclusion criteria for the respective studies, all subjects were healthy and none reported histories for any olfactory disturbances.
Odors were delivered using felt-tip pens (“Sniffin’ Sticks”) of approximately 14 cm length and an inner diameter of 1.3 cm. These pens carry a tampon soaked with 4 ml of liquid odorant. For odor presentation, the cap was removed from the pen for approximately 3 s, the pen’s tip brought in front of the subject’s nose and carefully moved from left to right nostril and backwards [3 (link)].
The threshold was obtained in a three alternative forced choice paradigm (3 AFC) where subjects were repeatedly presented with triplets of pens and had to discriminate one pen containing an odorous solution from two blanks filled with the solvent. Phenylethanol (dissolved in propylene glycol) or n-butanol (dissolved in water) were used, with both odorants having been found equivalent in olfactory sensitivity testing: scores obtained with both are correlated [17 (link)]. The highest concentration was a 4% odor solution. Sixteen concentrations were created by stepwise diluting previous ones by 1:2. Starting with the lowest odor concentration, a staircase paradigm was used where two subsequent correct identifications of the odorous pen or one incorrect answer marked a so-called turning point, and resulted in a decrease or increase, respectively, of concentration in the next triplet. Triplets were presented at 20 s intervals. The threshold score was the mean of the last four turning points in the staircase, with the final score ranging between 1 and 16 points.
The discrimination task used the same 3 AFC logic. Two pens of any triplet contained the same odorant, while the third pen smelled differently. Subjects were asked to indicate the single pen with a different smell. Within-triplet intervals were approximately 3 s. As the odors used in this subtest were more intense, between-triplets intervals were 20–30 s. The score was the sum of correctly identified odors. Hence, the scores in this task ranged from 0 to 16 points. Importantly, subjects were blindfolded for the threshold and discrimination tasks to avoid visual identification of target pens.
Odor identification comprised common and familiar odorants (recognized by at least 75% of the population). Subjects were presented with single pens and asked to identify and label the smell, using four alternative descriptors for each pen. Between-pen intervals were approximately 20–30 s. The total score was the sum of correctly identified pens, thus subjects could score between 0 and 16 points.
The final “TDI score” was the sum of scores for Threshold, Discrimination and Identification subtests, with a range between 1 and 48 points.
Publication 2018
Butyl Alcohol Discrimination, Psychology Feelings Females Hypersensitivity Males Nose Odorants Odors Phenylethyl Alcohol Propylene Glycol Sense of Smell Solvents Triplets
All procedures followed the Institute of Laboratory Animal Research guidelines and were approved by the Animal Care and Use Committee of the National Institute of Mental Health. Transgenic mice expressing HSV-TK under the GFAP promoter were generated from a previously-generated plasmid28 (link) using standard techniques and bred on a mixed C57Bl/6:CD-1 background. Male v-WT and v-TK mice were treated with valganciclovir for 8 weeks (dexamethasone experiment), 10-19 weeks (endocrine), 12 weeks (behavior) or 4 weeks (histology; histology after 12 weeks in Supplementary Fig. 1), beginning at 8 weeks of age. Male C57Bl/6 mice were irradiated under pentobarbital anesthesia, as described previously29 (link), and tested 9 weeks later. For immunohistochemical analyses, mice were given BrdU 6 weeks (for PVN analysis) or 24 hours prior to sacrifice, brain sections were immunostained as previously described29 (link), and labeled cells were counted stereologically.
Serum corticosterone was measured by radioimmunoassay (MP Biomedicals) from submandibular blood samples obtained directly from the home cage condition or after exploration of a novel box, restraint, or isoflurane exposure. For the dexamethasone suppression test, dexamethasone (Sigma; 50 μg/kg in propylene glycol) or vehicle were injected 90 min prior to restraint, and blood was sampled immediately following 10 min restraint.
Behavioral tests were performed following 30 min of restraint or directly from the home cage. Different cohorts of mice were tested in the NSF test, elevated plus maze, forced swim test and sucrose preference test as previously described.12 (link), 18 (link), 21 , 30 (link) Statistical analyses were performed by t-test, log-rank test, or ANOVA with Fisher's LSD test for post hoc comparisons. Significance was set at P<0.05.
Publication 2011
Anesthesia Animals Animals, Laboratory Behavior Test BLOOD Brain Bromodeoxyuridine Cells Corticosterone Dexamethasone Elevated Plus Maze Test Glial Fibrillary Acidic Protein Isoflurane Males Mice, Inbred C57BL Mice, Laboratory Mice, Transgenic neuro-oncological ventral antigen 2, human Pentobarbital Propylene Glycol Radioimmunoassay Serum Sucrose System, Endocrine Valganciclovir

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Publication 2013
Animals Central Nervous System Ethanol Hypersensitivity Injections, Intraperitoneal Intrathecal Injection Lumbar Region Mice, House Needles Nitroglycerin Normal Saline Pharmaceutical Preparations Propylene Glycol Sumatriptan Topiramate

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Publication 2009
Animals Biological Assay Dissection Formaldehyde Glucan 1,4-alpha-Glucosidase Glucose Glycerin Glycogen Larva Microscopy Microscopy, Confocal Propylene Glycol Proteins solvent red 27 Staining Student Triglycerides Tween 20
In whole-cell catalysis bioprocess, xylose, erythritol, 1,3-propylene glycol (1,3-PG), and 3-hydroxypropionic acid (3-HPA) were obtained from Aladdin. Xylonic acid (XA) was purchased from TRC-Canada, erythrulose and yeast extract were procured from Sigma. All other chemicals including nutrient salts and sodium alginate were of analytical grade and were commercially available.
The concentration of xylose and XA were detected by high-performance anion-exchange chromatography (HPAEC) coupled with pulsed amperometric detector (Thermo ICS-5000). NaOH (100 mM) was used as mobile phase at flow rate of 0.3 mL/min. The separation column used was CarboPac™ PA200. The titer of erythritol, erythrulose, 1,3-PG and 3-HPA were measured by high-performance liquid chromatography (HPLC) (Agilent 1100 series) equipped with Carbohydrate Ca++ 8um HyperRez XP Column and deionized water, after ultrasound, was used as mobile phase at 0.6 mL/min.
Five parallel assays were performed for each experiment.
Publication 2020
3-hydroxypropionaldehyde Anions Biological Assay Carbohydrates Catalysis Cells Chromatography Erythritol erythrulose High-Performance Liquid Chromatographies hydracrylic acid Nutrients Propylene Glycol Salts Sodium Alginate Ultrasonics xylonic acid Xylose Yeast, Dried

Most recents protocols related to «Propylene Glycol»

Not available on PMC !

Example 13

IngredientsQty/vial
Melphalan50mg
PG5ml
Ethanol5ml
0.1N NaOH/0.1N HCLQS

NLT 80% of batch volume ethanol was transferred into a manufacturing vessel.

Propylene glycol was added to a vessel containing ethanol. Melphalan was added to the above mixture. Check the pH of the sample and if required adjust the pH to 3.5-5.5 using 0.1N NaOH/0.1N HCL. Final batch volume was made up using ethanol. The obtained solution was filtered and filled in vials followed by capping and sealing. The formulation was tested for stability at 2-8° C. for a period of 1 Month. Stability data is summarized 13A.

TABLE 13A
Stability at 1 Month1 Month
Purity99.48
Maximum Individual impurity0.1
Total Impurities0.52

Although the formulations, compositions, schemes and methods of the present disclosure have been described with reference to exemplary embodiments thereof, the present disclosure is not limited thereby. Indeed, the exemplary embodiments are implementations of the disclosed methods are provided for illustrative and non-limitative purposes. Changes, modifications, enhancements and/or refinements to the disclosed methods may be made without departing from the spirit or scope of the present disclosure. Accordingly, such changes, modifications, enhancements and/or refinements are encompassed within the scope of the present invention. All publications, patent applications, patents, figures and other references mentioned herein are expressly incorporated by reference in their entirety.

Patent 2024
Blood Vessel Ethanol Melphalan Propylene Glycol

Example 1

S. NoIngredientsQuantity
1Levothyroxine sodium0.01-1 mg
2Arginine0.01-4 mg
3Propylene glycol0.01-1 ml
4Sodium hydroxideq.s
5Ultrapure waterq.s to 0.1-2 ml
Manufacturing Process

Ultrapure water was taken in a compounding vessel and arginine was added and stirred. Propylene glycol was added to the solution and stirred. pH of the solution was adjusted to 11±0.5 by the addition of sodium hydroxide solution. Then the bulk solution was cooled to 2° C. to 8° C. Levothyroxine sodium was added and stirred till a clear solution was obtained, while maintaining the temperature at 5±3° C. The solution was filtered, followed by filling into suitable containers.

Patent 2024
Arginine Blood Vessel Dietary Fiber hydroxide ion Levothyroxine Sodium Propylene Glycol Sodium Hydroxide Thyroxine

Example 5

Additional formulations which vary the amounts of transcutol and ethyl alcohol were examined by the same procedure.

Formulations tested (Table 4):

Formula
D1C
PENNSAID
2%FormulaFormulaFormulaFormula
DiclofenacD37D38D39D40
IngredientWt %Wt %Wt %Wt %Wt %
Oleic Acid08.08.08.08.0
DMSO45.516.021.016.021.0
Transcutol026.021.021.016.0
Sodium Diclofenac2.02.02.02.02.0
Propylene Glycol11.011.011.011.011.0
Poloxamer P18800000
Ethyl Alcohol31.3534.034.039.039.0
Hydroxypropyl3.03.03.03.03.0
Cellulose
Water7.150000
TOTAL100100100100100

FIGS. 9, 10, and 11 depict a head-to-head comparison of Pennsaid and Formulation D34 as a delivered transdermal dose, dose retained in the skin, and calculated as percent delivery of diclofenac.

Patent 2024
Acids Cyclooxygenase Inhibitors Diclofenac Diclofenac Sodium Ethanol Figs Head hydroxypropylcellulose Obstetric Delivery Oleic Acid Poloxamer Propylene Glycol Skin Sodium Sulfoxide, Dimethyl Transcutol

Example 4

Additional formulations which vary the amounts of oleic acid, propylene glycol, and ethyl alcohol were examined by the same procedure.

Formulations tested (Table 3):

Formula
D1C
PENNSAID
2%FormulaFormulaFormulaFormulaFormula
DiclofenacD51D52D53D54D55
IngredientWt %Wt %Wt %Wt %Wt %Wt %
Oleic Acid08.08.08.04.04.0
DMSO45.520.020.020.020.020.0
Transcutol024.524.524.524.524.5
Sodium Diclofenac2.02.02.02.02.02.0
Propylene Glycol11.011.06.03.011.03.0
Poloxamer P188000000
Ethyl Alcohol31.3531.536.539.535.543.5
Hydroxypropyl3.03.03.03.03.03.0
Cellulose
Water7.1500000
TOTAL100100100100100100

FIG. 7 depicts skin permeation delivered dose data for 2% diclofenac formulations from Table 1, while FIG. 8 depicts skin permeation flux data for 2% diclofenac formulations from Table 1. As shown, these formulae can deliver equivalent amounts of diclofenac to that of Formula D1C with substantially less DMSO and at a much lower amount of the formula applied.

Patent 2024
Acids Cyclooxygenase Inhibitors Diclofenac Diclofenac Sodium Ethanol hydroxypropylcellulose Oleic Acid Poloxamer Propylene Glycol Skin Sodium Sulfoxide, Dimethyl Transcutol

Example 3

Extrapolating from formulation D32, additional formulations which contained reduced amounts of DMSO and increased amounts of transcutol were examined by the same procedure.

Formulations tested (Table 2):

Formula
D1C
PENNSAID
2%FormulaFormulaFormula
DiclofenacD34D35D36
IngredientWt %Wt %Wt %Wt %
Oleic Acid08.08.08.0
DMSO45.521.021.021.0
Transcutol026.026.026.0
Sodium Diclofenac2.02.02.02.0
Propylene Glycol11.011.011.011.0
Poloxamer P18803.00.50
100% Ethyl Alcohol31.3526.028.529.0
Hydroxypropyl3.03.03.03.0
Cellulose
Water7.15000
TOTAL100100100100

FIGS. 3, 4 and 5 depict a head-to-head comparison of Pennsaid and Formulation D34 as a delivered transdermal dose, dose retained in the skin, and calculated as percent delivery of diclofenac. As can be seen, formulation D34 delivered significantly more diclofenac transdermally than did Pennsaid, while Pennsaid exhibited a greater amount retained in the epidermis and dermis. The percent transdermal delivery of diclofenac from formulation D34 was greater than 15% at 48 hours.

FIG. 6 shows the diclofenac flux over time for these two formulations. A maximum diclofenac flux was observed within 12 hours of application.

Patent 2024
Acids Cyclooxygenase Inhibitors Dermis Diclofenac Diclofenac Sodium Epidermis Ethanol Head hydroxypropylcellulose Obstetric Delivery Oleic Acid Poloxamer Propylene Glycol Skin Sodium Sulfoxide, Dimethyl Transcutol Vision

Top products related to «Propylene Glycol»

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Propylene glycol is a clear, colorless, and odorless liquid that is commonly used as a solvent and humectant in various industries. It has a wide range of applications, including in the manufacturing of pharmaceuticals, cosmetics, and food products. Propylene glycol exhibits low toxicity and is generally recognized as safe for certain applications.
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DMSO is a versatile organic solvent commonly used in laboratory settings. It has a high boiling point, low viscosity, and the ability to dissolve a wide range of polar and non-polar compounds. DMSO's core function is as a solvent, allowing for the effective dissolution and handling of various chemical substances during research and experimentation.
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Tween 80 is a non-ionic surfactant and emulsifier. It is a viscous, yellow liquid that is commonly used in laboratory settings to solubilize and stabilize various compounds and formulations.
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Methanol is a clear, colorless, and flammable liquid that is widely used in various industrial and laboratory applications. It serves as a solvent, fuel, and chemical intermediate. Methanol has a simple chemical formula of CH3OH and a boiling point of 64.7°C. It is a versatile compound that is widely used in the production of other chemicals, as well as in the fuel industry.
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Ethanol is a clear, colorless liquid chemical compound commonly used in laboratory settings. It is a key component in various scientific applications, serving as a solvent, disinfectant, and fuel source. Ethanol has a molecular formula of C2H6O and a range of industrial and research uses.
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Oil Red O is a fat-soluble dye used in histology and cell biology for the staining of neutral lipids, such as triglycerides and cholesterol esters. It is a useful tool for the identification and visualization of lipid-rich structures in cells and tissues.
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Labrasol is a non-ionic surfactant used in various pharmaceutical and cosmetic applications. It is a polyoxyethylene glycerol fatty acid ester that acts as a solubilizer, emulsifier, and wetting agent. Labrasol is designed to improve the solubility and bioavailability of active ingredients in formulations.
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Acetonitrile is a colorless, volatile, flammable liquid. It is a commonly used solvent in various analytical and chemical applications, including liquid chromatography, gas chromatography, and other laboratory procedures. Acetonitrile is known for its high polarity and ability to dissolve a wide range of organic compounds.
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Glycerol is a colorless, odorless, and viscous liquid used in various laboratory applications. It is a basic chemical compound with the molecular formula C₃H₈O₃. Glycerol is commonly used as a solvent, humectant, and stabilizer in many laboratory procedures.
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Sodium hydroxide is a chemical compound with the formula NaOH. It is a white, odorless, crystalline solid that is highly soluble in water and is a strong base. It is commonly used in various laboratory applications as a reagent.

More about "Propylene Glycol"

Propylene Glycol (PG) is a widely used chemical compound with diverse applications in various industries, including pharmaceuticals, cosmetics, and food production.
It is a clear, colorless, and odorless liquid that serves as a solvent, humectant, and antifreeze agent.
PG is commonly found in a variety of products, such as e-cigarette liquids, lotions, and certain medications.
Researchers and scientists often investigate the efficacy and safety of Propylene Glycol in different applications, focusing on its potential benefits and any possible side effects.
PG is often used in combination with other chemicals like DMSO, Tween 80, Methanol, Ethanol, Oil Red O, Labrasol, Acetonitrile, and Glycerol.
The versatility of Propylene Glycol makes it a valuable ingredient in formulations, and understanding its properties and interactions is crucial for optimizing research protocols and enhancing reproducibility.
PG's ability to act as a solvent, humectant, and antifreeze agent makes it a useful additive in various industries.
In the pharmaceutical and cosmetic sectors, it is employed as a carrier for active ingredients, helping to improve their bioavailability and stability.
In the food industry, PG is used as a preservative and to enhance flavor and texture.
When conducting research involving Propylene Glycol, it's important to consider related terms and abbreviations, such as PG, to ensure comprehensive literature searches and data analysis.
Additionally, understanding the properties and interactions of PG with other chemicals, like DMSO and Glycerol, can help researchers design more effective and reproducible experiments.
By leveraging the insights gained from the MeSH term description and the capabilities of PubCompare.ai's AI-driven comparison platform, researchers can optimize their research protocols and enhance the reproducibility of their findings related to Propylene Glycol and its diverse applications.