• Corpus ID: 15249552

A REVIEW ON APPLICATIONS OF MALTODEXTRIN IN PHARMACEUTICAL INDUSTRY

@inproceedings{Parikh2014ARO,
  title={A REVIEW ON APPLICATIONS OF MALTODEXTRIN IN PHARMACEUTICAL INDUSTRY},
  author={Aakash Parikh and Siddharth Agarwal and Kirtesh Raut},
  year={2014}
}
Since in a formulation excipient affects the critical properties of formulation such as stability and bioavailability it was mandatory to evaluate a safe and inert excipient for its versatility. Maltodextrin which is obtained bypartial hydrolysis of starch is water soluble, non-sweetproduct due to which it is used as diluents in tablets and coating material in microencapsulation of various sensitive nutraceuticals like vitamins has other applications in pharmaceutical industry as well… 

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References

SHOWING 1-10 OF 36 REFERENCES

Maltodextrin fast dissolving films for quercetin nanocrystal delivery. A feasibility study.

Comparative Study of Carriers Used in Proniosomes

Comparison of carriers of proniosomes involves comparison of such carriers and criteria for selection of suitable carrier for the preparation of the proniosome-derived niosomes.

Fast dissolving films made of maltodextrins.

FORMULATION AND EVALUATION OF MALTODEXTRIN BASED PRONIOSOMES LOADED WITH INDOMETHACIN

The niosomal formulation could be a promising delivery system for indomethacin with improved bioavailability and prolonged drug release profile with in vivo performance evaluation.

A REVIEW ON PRONIOSOME, A PROMISING CARRIER FOR DELIVERY OF DRUG ACROSS MEMBRANES

The latest approach in the field of vesicular delivery is to combine the two previously mentioned techniques by extending the pro-vesicular approach to niosomes through the formation of ‘‘proniosomes’’.

Coprocessing via spray drying as a formulation platform to improve the compactability of various drugs.

Preparation of Fast Dissolving Films for Oral Dosage from Natural Polysaccharides

Fast-dissolving films (FDFs) prepared from polysaccharides could be promising candidates as oral dosage forms containing drugs, and would be expected to show drug dissolution in the oral cavity.

FORMULATION AND EVALUATION OF IBUPROFEN LOADED MALTODEXTRIN BASED PRONIOSOME

Ibuprofen loaded maltodextrin based proniosome were prepared by slurry method with different surfactan t to carrier ratio. The proniosome formulation was evaluated for FT-IR study and scanning