Abstract

Cellulose based polymers have shown tremendous potential as drug delivery carrier for oral drug delivery system (DDS). Hydroxyethyl cellulose (HEC) and hydroxypropyl cellulose (HPC) are widely explored as excipients to improve the solubility of poorly water soluble drugs and to improve self-life of dosage form. This work is an attempt to modulate the physicochemical properties of these cellulose derivatives using biofield treatment. The treated HEC and HPC polymer were characterized by X-ray diffraction (XRD), differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The XRD studies revealed a semi-crystalline nature of both the polymers. Crystallite size was computed using Scherrer’s formula, and treated HEC polymer showed a significant increase in percentage crystallite size (835%) as compared to the control polymer. This higher increase in crystallite size might be associated with greater crystallite indices causing a reduction in amorphous regions in the polymer. However treated HPC polymer showed decrease in crystallite size by -64.05% as compared to control HPC. DSC analysis on HEC polymer revealed the presence of glass transition temperature in control and treated HEC polymer. We observed an increase in glass transition temperature in treated HEC, which might be associated with restricted segmental motion induced by biofield. Nonetheless, HPC has not showed any glass transition. And no change in melting temperature peak was observed in treated HPC (T2) however melting temperature was decreased in T1 as compared to control HPC. TGA analysis established the higher thermal stability of treated HEC and HPC. CHNSO results showed significant increase in percentage oxygen and hydrogen in HEC and HPC polymers as compared to control samples. This confirmed that biofield had induced changes in chemical nature and elemental composition of the treated polymers (HEC and HPC).

Highlights

  • The oral route is by far the most preferred and convenient route for delivery of many pharmaceutically active drugs

  • CHNSO analysis was carried out to investigate the elemental composition in the treated Hydroxyethyl cellulose (HEC) and hydroxypropyl cellulose (HPC) polymers

  • X-ray diffraction (XRD) showed that treatment with biofield had significantly enhanced the crystallite size by 835% in treated HEC as compared to control and possibly this increased the crystallinity

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Summary

Introduction

The oral route is by far the most preferred and convenient route for delivery of many pharmaceutically active drugs. Oral drug delivery is an excellent non-invasive approach that provides alternative to invasive routes such as intravenous, intramuscular, subcutaneous administration of drugs. It provides several challenges for pharmaceutical scientist investigating novel delivery techniques to overcome. There are different formulations strategies including sprays, tablets, mouthwashes, gels, pastes and patches are currently used for delivery into and across the oral mucosa. There are a small number of drugs which are routinely delivered via the sublingual or buccal route e.g. systemic delivery of glyceryl trinitrate for angina relief and topical corticosteroid administration for inflammatory diseases of the oral mucosa including lichen planus [2]. More time/pH controlled DDS should be designed to overcome these obstacles

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