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Amberlite Irp64

Amberlite irp 64 Resin description

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0% found this document useful (0 votes)
214 views5 pages

Amberlite Irp64

Amberlite irp 64 Resin description

Uploaded by

Noemi
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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AMBERLITE™ IRP64 Pharmaceutical Grade Cation Exchange Resin

(Polacrilex Resin)

Description

AMBERLITE IRP64[1] resin is an insoluble, weakly acidic, hydrogen form, cation exchange resin supplied as a dry,
fine powder. AMBERLITE IRP64 resin is suitable for use in pharmaceutical applications, primarily as a carrier for
certain basic (cationic) drugs and related substances. It is also used to mask objectionable tastes associated with
certain basic drugs. Commercial examples of its use include:

z Stabilization of Vitamin B12


z Sustained Release of Nicotine

A Drug Master File for this product is maintained with the United States Food and Drug Administration. Letters of
authorization granting access to the file by FDA in support of NDA and ANDA submittals will be provided upon
request. Similar assistance can also be offered in support of the registration of formulations containing AMBERLITE
IRP64 in many other countries. AMBERLITE IRP64 resin is manufactured in accordance with Good Manufacturing
Practices (cGMP) for bulk pharmaceutical chemicals.

Identification

AMBERLITE IRP64 resin can be identified by infrared spectroscopy, as shown in the sample spectrum in Fig. 1.

Table 1: Typical Properties


These properties are typical but do not constitute specifications.

Ionic form Hydrogen


Appearance White to off white fine powder free of foreign matter
and any agglomeration
IR Identification Conforms to reference spectrum assay
Exchange capacity «as is Not less than 10.0 meq/g, on dried basis
Purify testing
Sodium Not more than 0.20 %
Heavy metals Not more than 0.001 %
Iron Not more than 0.01 %
Methacrylic acid Not more than 300 ppm
Water extractable impurities Not more than 2.0 %
Physico-chemical testing
Loss on drying Not more than 5.0 %
Particle size
> 0.150 mm Not more than 1.0 %
> 0.075 mm 15. 0 to 30.0 %
> 0.050 mm Not more than 70.0 %
Microbial purity
Total bacterial count Not more than 100 cfu/g
Total mold count Not more than 100 cfu/g
[1]
The use of AMBERLITE pharmaceutical grade ion exchange resins as components of drug
formulations is subject to the Food, Drug, and Cosmetic Act as amended.

Chemical Structure

AMBERLITE IRP64 resin is derived from a porous copolymer of methacrylic acid and divinylbenzene. The chemical
structure of AMBERLITE IRP64 is shown in Figure 2.

Applications

Applications for AMBERLITE IRP64 resin include:

z Taste Masking
z Drug Stabilization
z Carrier for Cationic Drugs
z Controlled Release Formulations
AMBERLITE IRP64 resin provides a means for binding medicinal agents onto an insoluble polymeric matrix. This
affords an effective technique for overcoming problems of taste and odor in oral dosage formulations as well as
providing a matrix upon which a sustained or controlled release formulation can be developed.

The high affinity of AMBERLITE IRP64 resin for the hydrogen ion results in ready desorption of adsorbed species by
exposure to an acidic environment, such as that exhibited in the stomach. This accounts for the higher desorption
efficiencies versus a strong acid cation resin like AMBERLITE IRP69.

Chemical instability problems can sometimes be resolved by adsorption on to AMBERLITE IRP64 resin. For
example, complexes of AMBERLITE IRP64 resin with cyanocobalamin (Vitamin B12), a nonionic material, have
been used for many years as a means of providing a stable oral dosage form of this vitamin.

Drug Loading

Batch equilibration is the preferred practice when loading a drug or other sorbate into finely divided ion exchange
operations normally used with ion exchange resins, resin powders. Due to its fine particle size, AMBERLITE IRP64
resin does not lend itself to conventional columnar operations normally used with ion exchange resins.

The mobile, or exchangeable, cation in IRP64 resin is the hydrogen ion. In acidic environments (generally below
pH 4) AMBERLITE IRP64 resin exists as the free acid in an essentially nonionic state. Adsorption (loading) onto this
cation exchange resin is usually carried out at pH 6 or higher.

The amount of drug loaded onto AMBERLITE IRP64 resin will be influenced by such factors as:

z The inherent affinity or selectivity between the ion exchange resin and the drug.
z The concentration of the drug in the loading solution.
z The concentration and selectivity of competing cations.
z The pH of the loading solution.

The rate of loading will be affected by the activity of the drug and its molecular dimensions as well as the extent to
which the polymer phase is swollen during loading.

When utilizing a batch or equilibrium contact to load a drug or other anionic sorbate onto AMBERLITE IRP64 resin,
it may be desirable to load as much as possible of the substance of value onto the resin. Complete transfer of the
drug from the loading solution is not likely in a single equilibrium stage. Accordingly, more than one equilibration
may be required in order to achieve the desired loading onto the resin. The use of two or more loading stages,
separating the resin from the liquid phase between stages, is an effective means of achieving maximum loading of
the drug onto the resin while maintaining minimum loss of drug from the liquid phase of the final stage.

Carefully controlled laboratory experiments are required to establish precise loading and elution conditions.

Drug Release

The rate and completeness of drug desorption in vivo will be controlled by the diffusion rate of the drug through
the polymer phase of the resin, (usually a function of molecular weight), the selectivity of the drug for the resin,
and the concentration of electrolytes particularly in the hydrogen ion, in the desorption environment.

More hydrophobic drugs will usually elute from the resin at a lower rate, as will drugs with a relatively high
selectivity for the carboxylic acid functional structure in the resin. Other resin-sorbate interactions are possible,
and these can have a pronounced effect upon loading capacities and rates.

An example of this might be the presence of a transition metal in the structure of the sorbate molecule which can
result in considerable selectivity through the formation of a coordination compound with the resin.
Safe Handling Information

Material Safety Data Sheets (MSDS) are available for all Rohm and Haas products. These sheets contain pertinent
information that you may need to protect your employees and customers against any known health or safety
hazards associated with our products. We recommend that you obtain copies of our MSDS by calling 1-800-RH-
AMBER before using our products in your facilities. We also suggest that you contact your suppliers of other
materials recommended for use with our products for appropriate health and safety precautions before using
them.

Caution: Acidic and basic regenerant solutions are corrosive and should be handled in a manner that will prevent
eye and skin contact. In addition, the hazards of other organic solvents should be recognized and steps taken to
control exposure.

Nitric acid and other strong oxidizing agents can cause explosive reactions when mixed with ion exchange resins.
Proper design of process equipment to prevent rapid buildup of pressure is necessary if use of an oxidizing agent
such as nitric acid is contemplated. Before using strong oxidizing agents in contact with ion exchange resins,
consult sources knowledgeable in the handling of these materials.

Note: Ion exchange resins and polymeric adsorbents, as produced, contain by-products resulting from the
manufacturing process. The user must determine the extent to which organic by-products must be removed for
any particular use and establish techniques to assure that the appropriate level of purity is achieved for that use.
The user must ensure compliance with all prudent safety standards and regulatory requirements governing the
application. Except where specifically otherwise stated, Rohm and Haas Company does not recommend its ion
exchange resins or polymeric adsorbents as supplied as being suitable or appropriately pure for any particular use.
Consult your Rohm and Haas technical representative for further information.

Amberlite IRP64 Applications Reference List

Controlled/Sustained Release

Leo Corporation, 1973. Smoking substitutes and method of production. Patent GB 1,325,011.

Taste-Masking

Douglas, S.J. Glaxo Group Research Ltd, 1990. Process for the preparation of a ranitidine resin absorbate. US
5219 563.

Astruc, J., and A. Sambot, 1970. Ion-exchange resin: spiramycin compositions. Patent GB 1,180,233.

Borodkin, S., and D.P. Sundberg, 1971. Chewable tablets including coated particles of psuedoephedine- weak
cation exchange resin. Patent US 3,594,470.

Other

Fretland, D.J., 1974. Use of ion-exchange resins for removing prostaglandins from human urine prior to
radioimunoassay. Prostaglandins 6 (5): 421-425.

Miles Laboratories, Inc., 1970 Detection device for enzymes and other factors in body fluids. Patent US 3,616,251.

All our products are produced in ISO 9001 certified manufacturing facilities.
AMBERLITE is a trademark of Rohm and Haas Company, Philadelphia, U.S.A.

Ion exchange resins and polymeric adsorbents, as produced, contain by-products resulting from the manufacturing process. The user must
determine the extent to which organic by-products must be removed for any particular use and establish techniques to assure that the
appropriate level of purity is achieved for that use. The user must ensure compliance with all prudent safety standards and regulatory
requirements governing the application. Except where specifically otherwise stated, Rohm and Haas Company does not recommend its ion
exchange resins or polymeric adsorbents, as supplied, as being suitable or appropriately pure for any particular use. Consult your Rohm and
Haas technical representative for further information. Acidic and basic regenerant solutions are corrosive and should be handled in a manner
that will prevent eye and skin contact. Nitric acid and other strong oxidising agents can cause explosive type reactions when mixed with ion
exchange resins. Proper design of process equipment to prevent rapid buildup of pressure is necessary if use of an oxidising agent such as
nitric acid is contemplated. Before using strong oxidising agents in contact with ion exchange resins, consult sources knowledgeable in the
handling of these materials.

Rohm and Haas Company makes no warranties either expressed or implied as to the accuracy of appropriateness of this data and expressly
excludes any liability upon Rohm and Haas arising out of its use. We recommend that the prospective users determine for themselves the
suitability of Rohm and Haas materials and suggestions for any use prior to their adoption. Suggestions for uses of our products of the
inclusion of descriptive material from patents and the citation of specific patents in this publication should not be understood as
recommending the use of our products in violation of any patent or as permission or license to use any patents of the Rohm and Haas
Company. Material Safety Data Sheets outlining the hazards and handling methods for our products are available on request.

©Rohm and Haas, 2006 All rights reserved. February 2006

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