Evaluation Of oil extract from T. catappa as a sustained release injection base

Terminalia catappa seed oil with the following parameters: specific gravity-0.9200 ± 0.10. refractive index-0.4640 ± 0.06, viscosity (cps)-36.80 ± 0.94, peroxide value-8.63 ± 0.03. saponification value-157.8 ± 2.88), iodine value-38.63 ± 1.06 was used to formulate haloperidol in injection dosage form of 10 mg/2 ml. The formulation was evaluated for content of active ingredient, stability, toxicity, physicochemical properties and release patterns through dialysis membrane in phosphate buffer at physiologic pH of 7.4. The results were compared with those of a standard haloperidol injection B.P. Active ingredient content was found to be 100.61 ± 0.38 and 101.29 ± 0.64 percent (%) for the oil injection and the B.P formulation, respectively. They all showed requisite sterility as no organisms were isolated after incubation for seven (7) days in appropriate media and temperature. However, there was a significant delay i the release of haloperidol from the oil injection as against the standard B.P injection (P<0.05) The haloperidol oil injection exhibited sustained release behavior and had a predicted shelf life of 2.66 years compared to the 1.65 years evaluated for the haloperidol injection B.P.

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Publication Details

Journal
JORMAR
Published
2026-11-11
DOI
https://doi.org/10.83043/aa18qy27
Primary Topic
Advanced Drug Delivery Systems
Type
article
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article

Evaluation Of oil extract from T. catappa as a sustained release injection base

Okide Gb, U Ajali, E. O. Omeje, WO Obonga et al.
JORMAR
Advanced Drug Delivery Systems
article

Evaluation Of oil extract from T. catappa as a sustained release injection base

Okide Gb, U Ajali, E. O. Omeje, WO Obonga, C.O. Esimone
article en

Abstract

Terminalia catappa seed oil with the following parameters: specific gravity-0.9200 ± 0.10. refractive index-0.4640 ± 0.06, viscosity (cps)-36.80 ± 0.94, peroxide value-8.63 ± 0.03. saponification value-157.8 ± 2.88), iodine value-38.63 ± 1.06 was used to formulate haloperidol in injection dosage form of 10 mg/2 ml. The formulation was evaluated for content of active ingredient, stability, toxicity, physicochemical properties and release patterns through dialysis membrane in phosphate buffer at physiologic pH of 7.4. The results were compared with those of a standard haloperidol injection B.P. Active ingredient content was found to be 100.61 ± 0.38 and 101.29 ± 0.64 percent (%) for the oil injection and the B.P formulation, respectively. They all showed requisite sterility as no organisms were isolated after incubation for seven (7) days in appropriate media and temperature. However, there was a significant delay i the release of haloperidol from the oil injection as against the standard B.P injection (P<0.05) The haloperidol oil injection exhibited sustained release behavior and had a predicted shelf life of 2.66 years compared to the 1.65 years evaluated for the haloperidol injection B.P.

JORMAR
University of Nigeria (NG)
Advanced Drug Delivery Systems
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