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Merck
  • Continuous API-crystal coating via coacervation in a tubular reactor.

Continuous API-crystal coating via coacervation in a tubular reactor.

International journal of pharmaceutics (2014-08-12)
M O Besenhard, A Thurnberger, R Hohl, E Faulhammer, J Rattenberger, J G Khinast
초록

We present a proof-of-concept study of a continuous coating process of single API crystals in a tubular reactor using coacervation as a microencapsulation technique. Continuous API crystal coating can have several advantages, as in a single step (following crystallization) individual crystals can be prepared with a functional coating, either to change the release behavior, to protect the API from gastric juice or to modify the surface energetics of the API (i.e., to tailor the hydrophobic/hydrophilic characteristics, flowability or agglomeration tendency, etc.). The coating process was developed for the microencapsulation of a lipophilic core material (ibuprofen crystals of 20 μm- to 100 μm-size), with either hypromellose phthalate (HPMCP) or Eudragit L100-55. The core material was suspended in an aqueous solution containing one of these enteric polymers, fed into the tubing and mixed continuously with a sodium sulfate solution as an antisolvent to induce coacervation. A subsequent temperature treatment was applied to optimize the microencapsulation of crystals via the polymer-rich coacervate phase. Cross-linking of the coating shell was achieved by mixing the processed material with an acidic solution (pH<3). Flow rates, temperature profiles and polymer-to-antisolvent ratios had to be tightly controlled to avoid excessive aggregation, leading to pipe plugging. This work demonstrates the potential of a tubular reactor design for continuous coating applications and is the basis for future work, combining continuous crystallization and coating.

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Supelco
Dehydrated Alcohol, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
Hydrogen chloride solution, 3 M in cyclopentyl methyl ether (CPME)
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Acetic acid-12C2, 99.9 atom % 12C
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Ethanol solution, certified reference material, 2000 μg/mL in methanol
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Ibuprofen, Pharmaceutical Secondary Standard; Certified Reference Material
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di-Sodium hydrogen phosphate dihydrate, BioXtra, ≥98.0% (T)
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Sodium sulfate, BioUltra, anhydrous, ≥99.0% (T)
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Acetic acid, analytical standard
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Ibuprofen
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Hydrochloric acid solution, 32 wt. % in H2O, FCC
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Hydrochloric acid, puriss., 24.5-26.0%
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Sodium sulfate, puriss., meets analytical specification of Ph. Eur., BP, USP, anhydrous, 99.0-100.5% (calc. to the dried substance)
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Hydrochloric acid, ACS reagent, 37%
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Sodium sulfate, ACS reagent, ≥99.0%, anhydrous, powder
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Acetic acid, glacial, ACS reagent, ≥99.7%
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Hydrogen chloride solution, 1.0 M in acetic acid
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Acetic acid, glacial, puriss., meets analytical specification of Ph. Eur., BP, USP, FCC, 99.8-100.5%
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di-Sodium hydrogen phosphate dihydrate, puriss. p.a., reag. Ph. Eur., 98.5-101.0% (calc. to the dried substance)
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