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Supplier: BMT USA, LLC
Description: BMT Stability Chambers and Incubators principle of operation is based on a precise forced air circulation combined with a patented powerful cooling system and a humidifier situated in the chamber. A multiprocessor humidifying and dehumidifying control system together with a powerful illumination
- Configuration: Benchtop / Instrument, Reach-In
- Chamber Capacity: 29.17 gallons
- Test Parameters: Temperature, Humidity
- Temperature Control: Heating, Cooling
Supplier: Quantachrome Instruments
Description: Water sorption behavior plays an important role in the development and use of many common and advanced materials. Some examples include: Stability of pharmaceutical excipients and drug actives Drying and storage of grains Texture and shelf life of food products PEM fuel cell components Mortar
- Property Analyzed: Absorption / Water Absorption, Porosimetry / Pore Volume
- Test Media / Material: Adhesives / Coatings, Ceramics / Glass, Concrete / Cement, Food / Drugs, Powders / Granular Materials, Textiles
- Display & Special Features: Laboratory / Batch
Supplier: Fritsch GmbH - Milling and Sizing
Description: throughput Wear-free rotor made of stainless steel capable of accepting extreme loads Wear-free labyrinth seal between grinding chamber and drive motor High speed stability even under full load Conversion kit for iron-free grinding Equipment As a standard you receive the Variable Speed RotorShow More
Grinding Mills and Pulverizers - Rotor / Beater Mill -- Variable-Speed Rotor Mill PULVERISETTE 14 Classic LineSupplier: Fritsch GmbH - Milling and Sizing
Description: with extremely high air throughput Wear-free rotor made of stainless steel capable of accepting extreme loads Wear-free labyrinth seal between grinding chamber and drive motor High speed stability even under full load Conversion kit for iron-free grinding Equipment As a standard you receive
- Industry or Material Processed: Chemicals / Fertilizers, Construction Materials / Cement, Food Processing / Grain, Pharmaceutical / Cosmetics, Wood / Pulp & Paper, Polymers, Power / Coal & Coke, Waste / Recycling
- Scale / Capacity: Lab / Pilot
- Process Type: Dry
- Feed: Batch
Supplier: Caron Products and Services, Inc.
Description: technical innovations. These units have a wide temperature and humidity range and are designed in accordance with ICH Q1A guidelines, making them perfect for pharmaceutical stability drug testing. Caron's Environmental Test Chambers are also ideal for numerous other applications, such as shelfShow More
Description: accommodated. Changes in sample mass of 0.1μg and unrivalled long-term stability are hallmarks of the Intrinsic and which are required for the accurate measurement of water sorption phenomena. These measurements may take from a few minutes to a few hours to complete depending upon the sample size
- Property Analyzed: Adsorption / Desorption (Chemisorption/ Physisorption)
- Test Media / Material: Building & Construction Materials, Concrete / Cement, Food / Drugs, Porous Materials (Filters, Foam, etc.), Rock / Aggregate, Wood / Wood Product
- Display & Special Features: Computer Interface / Networkable, Laboratory / Batch
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Practical tips for better stability monitoring
New Webinar - Stability Studies & Stability Chamber Monitoring. Join us June 1, 2016, 9 AM EDT (UTC -4). Vaisala Regulatory Expert Piritta Maunu has created a new 1-hour training on best practices for stability testing in drug production. Piritta will outline five practical tips for better stability monitoring, including: what your stability studies need, best practices for your mapping qualification studies, proper use of mean kinetic temperature, how to handle incidents... (read more)
Browse Instructional Seminars and Training Services Datasheets for Vaisala
Gravimetric Water Vapor Sorption Analyzers
watch > > >The Aquadyne DVS: a short introduction. Gravimetric Water Vapor Sorption Analyzers. Water content, water sorption kinetics, and percent water uptake are all characteristics of interest to material scientists. Water sorption behavior plays an important role in the development and use of many common and advanced materials. . Stability of pharmaceutical excipients and drug actives . Drying... (read more)
Browse Property Testing Equipment Datasheets for Quantachrome Instruments
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In vitro and in vivo evaluation of single-unit commercial conventional tablet and sustained-release capsules compared with multiple-unit polystyrene microparti...
Stability studies were conducted on polystyrene micro- particles containing 30% wt/wt ibuprofen to assess drug stability with respect to drug content and drug release char- acteristics after storing the multiple-unit formulation in drug stability testing chambers (Campbell Electronics, Mumbai, India) at …
Moisture / Chambers
Steady State - Food Drug Stability Test Chamber .
Moisture / Humidity / Temperature Humidity Chambers
Steady State - Food Drug Stability Test Chamber .
Complexation of capsaicin with β-cyclodextrins to improve pesticide formulations: effect on aqueous solubility, dissolution rate, stability and soil adsorption
Samples for photochemical stability study were stored in a SYW-160B drug stability test chamber (Ningbo Science Equipment Ltd, Ningbo, China) equipped with a white fluorescent lamp (rapid-start type 20 W).
Comparison of Spray Freeze Drying and the Solvent Evaporation Method for Preparing Solid Dispersions of Baicalein with Pluronic F68 to Improve Dissolution and ...
The samples (∼200 mg), packed in glass vials with silica gel desiccant, were stored in a drug stability test chamber at 40°C and analyzed initially and after 1 to 6 months for baicalein content and dissolution by HPLC analysis.
Essential Elements for a GMP Analytical Chemistry Department
1.1 Purpose of the stability studies 1.2 Description of material (Drug Substance/ Drug Product) 1.3 Equipment ( Stability Chambers , Stability Data System, etc.) 1.4 Proposed Shelf Life 1.5 Guidelines followed 1.6 Stability Study Protocols 1.7 Statistical …
A hot‐melt extruded intravaginal ring for the sustained delivery of the antiretroviral microbicide UC781
To evalu- ate the chemical stability of UC781 in each extru- date group, samples were removed from the stability chambers and subjected to drug extractions at 11, 20, and 30 days.
Influence of Formulation and Processing Factors on Stability of Levothyroxine Sodium Pentahydrate
The drug substance was placed in stability chamber under various conditions as described in the “MATERIALS AND METHODS” section.
Analytical technology aided optimization and scale‐up of impinging jet mixer for reactive crystallization process
Color grade data were obtained by drug accelerated test using a stability chamber (Labonce-60GS) and a UV instrument (SHIMADZU UVmini-1240) was used to determine the transmittance.
Generic Development of Topical Dermatologic Products: Formulation Development, Process Development, and Testing of Topical Dermatologic Products
Additionally, the firm should be aware of the issue of physical orientation of stability samples in stability chambers , especially for a drug product with low viscosity.
Methotrexate-loaded biodegradable nanoparticles: preparation, characterization and evaluation of its cytotoxic potential against U-343 MGa human neuronal gliob...
2.3e DSC studies: Closed vials containing drug excipient blends were charged in stability chamber at 25 °C/60% RH for a period of 1 month and observed for change in physical attributes.
Development and in vitro evaluation of a flow-adjustable elastic drug infusion pump.
Passive-type drug infusion pumps have several advantages over active-type pumps including a simple drug chamber structure and relatively high operational stability .
Stressed Kinetics of Nanoemulsion Formulation Encapsulated Ropinirole with a Validated Ultra High Performance Liquid Chromatography–Synapt Mass Spectrometry (U...
No decomposition was detected on exposure of drug solution to light in a photo stability cham- ber (Fig not given).
Cardiac rehabilitation in patients
with implantable defibrillators
Using addi- tional detection criteria (onset, stability , dual- cham- ber algorithms) and optimized drug therapy, the number of inappropriate therapies may be reduced from 10% to 25% to less than 5% (15–17).