BPC-157 Capsules 500mcg

Oral research format of Body Protection Compound peptide. Capsules suit chronic-dosing study designs and gut-localized delivery models, where BPC-157's effects on intestinal-tract tissue have been investigated in published preclinical literature. HPLC-tested, third-party COA per batch.

$99.00

SKU: OM-CAPS-BPC157-500MCG Category:

Description

BPC-157 (Body Protection Compound-157; CAS 137525-51-0) is a synthetic 15-amino-acid peptide (sequence: GEPPPGKPADDAGLV) derived from a protective protein originally isolated from human gastric juice. Peer-reviewed research has investigated BPC-157 across animal models and in vitro cell-culture systems, with published studies appearing in journals including the Journal of Molecular Medicine, the Journal of Applied Physiology, and the Journal of Orthopaedic Research.

In a 2017 study published in the Journal of Molecular Medicine, Hsieh and colleagues reported that BPC-157 promoted angiogenesis in chick chorioallantoic membrane and endothelial tube-formation assays and accelerated blood-flow recovery in a rat hindlimb ischemia model, with the effect attributed to activation of the VEGFR2-Akt-eNOS signaling pathway [1].

Important Note on the Evidence Base

Important note on the evidence base: The published research on BPC-157 consists predominantly of animal-model studies (primarily rats) and in vitro cell-culture experiments. A Phase I safety study and a Phase II ulcerative colitis trial of the BPC-157 formulation PL 14736 were conducted by the Croatian pharmaceutical company Pliva, but full peer-reviewed Phase II efficacy results have not been published. The studies summarized below are preclinical and should be interpreted accordingly.

Published Research on BPC-157

The following peer-reviewed studies are summarized below. Full citations and direct links to each publication appear in the References section. Each summary identifies the experimental model used.

Angiogenesis & VEGFR2 Mechanism — Hsieh et al., Journal of Molecular Medicine (2017)

Hsieh and colleagues investigated the pro-angiogenic effects of BPC-157 across multiple experimental systems: a chick chorioallantoic membrane (CAM) assay, an endothelial tube-formation assay, and a rat hindlimb ischemia model assessed by laser Doppler scanning. The study sought to clarify the molecular pathway underlying BPC-157’s reported tissue-repair effects.

The authors observed that BPC 157 promotes angiogenesis in CAM assay and tube formation assay, with corresponding acceleration of blood-flow recovery and increased vessel density in the ischemic rat hindlimb model [1]. The investigators attributed the angiogenic effect to upregulation of vascular endothelial growth factor receptor 2 (VEGFR2) and activation of the Akt–endothelial nitric oxide synthase (eNOS) signaling pathway.

Read the full study: Therapeutic Potential of Pro-Angiogenic BPC157 is Associated with VEGFR2 Activation and Up-Regulation (J Mol Med 2017).

Tendon Fibroblast Outgrowth — Chang et al., Journal of Applied Physiology (2011)

Chang and colleagues conducted an in vitro study using tendon fibroblasts isolated from the Achilles tendons of male Sprague-Dawley rats. The investigators evaluated tendon-explant outgrowth, fibroblast proliferation (MTT assay), cell survival under hydrogen peroxide oxidative stress, and fibroblast migration (transwell filter migration assay) in the presence and absence of BPC-157.

The authors reported that BPC 157 significantly accelerated the outgrowth of tendon explants and amount-dependently increased the in vitro migration of tendon fibroblasts [2]. While direct cell proliferation was not significantly altered, fibroblast survival under oxidative stress was significantly enhanced in BPC-157-treated cultures compared with controls.

Read the full study: The Promoting Effect of Pentadecapeptide BPC 157 on Tendon Healing Involves Tendon Outgrowth, Cell Survival, and Cell Migration (J Appl Physiol 2011).

Achilles Tendon-to-Bone Healing — Krivic et al., Journal of Orthopaedic Research (2006)

Krivic and colleagues, working at the Laboratory for Experimental Surgery at the University of Zagreb Medical School, conducted a controlled rat study examining BPC-157’s effect on Achilles tendon-to-bone healing. The investigators surgically detached the Achilles tendon from its calcaneal insertion in rats — an injury that does not heal spontaneously — and assessed recovery with and without BPC-157 administration.

The authors reported that BPC 157 alone (without carrier) ameliorates healing of tendon and bone in the experimental rat model, with macroscopic, microscopic, and biomechanical assessments showing recovery of the tendon-to-bone unit that was not observed in untreated controls [3]. The study also examined corticosteroid-induced healing impairment and reported that BPC-157 opposed the aggravating effects of methylprednisolone.

Read the full study: Achilles Detachment in Rat and Stable Gastric Pentadecapeptide BPC 157 (J Orthop Res 2006).

Medial Collateral Ligament Healing — Cerovecki et al., Journal of Orthopaedic Research (2010)

Cerovecki and colleagues conducted a controlled rat study evaluating BPC-157 in medial collateral ligament (MCL) healing following surgical transection. Investigators administered BPC-157 by three routes — intraperitoneal injection, oral administration in drinking water, and topical application as a thin cream layer — with assessment over a 90-day post-injury period.

The authors reported that they improved medial collateral ligament (MCL) healing throughout 90 days after surgical transection using BPC-157 administered without a carrier [4]. Healing was evaluated by macroscopic appearance, microscopic histology, and biomechanical testing across the 90-day timeline.

Read the full study: Pentadecapeptide BPC 157 (PL 14736) Improves Ligament Healing in the Rat (J Orthop Res 2010).

About the Compound

BPC-157 is a synthetic 15-amino-acid peptide with the sequence Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val (GEPPPGKPADDAGLV). It represents a partial sequence of a larger protein known as Body Protection Compound (BPC), originally isolated from human gastric juice. Unlike many peptides used in research, BPC-157 has been described in the published literature as stable in human gastric juice without enzymatic degradation, and as effective in research models when administered without a delivery carrier.

The molecule was advanced into clinical development by the Croatian pharmaceutical company Pliva under the designations PL-10, PLD-116, and PL 14736 for inflammatory bowel disease research; published Phase I safety data in healthy volunteers were reported in conference proceedings, while completed Phase II efficacy results have not appeared in peer-reviewed literature.

  • CAS Number: 137525-51-0
  • Molecular Formula: C62H98N16O22
  • Molecular Weight: 1419.55 g/mol
  • Sequence: GEPPPGKPADDAGLV
  • Synonyms: Body Protection Compound-157, BPC-157, PL-10, PLD-116, PL 14736, Bepecin
  • Mechanisms investigated in research literature: VEGFR2-mediated angiogenesis; Akt–eNOS signaling; nitric oxide system modulation; growth-hormone-receptor upregulation; fibroblast migration and survival

Product Specifications

Omnix Peptides supplies BPC-157 as encapsulated material in sealed amber bottles intended exclusively for in vitro laboratory research. Each production lot is independently characterized using high-performance liquid chromatography (HPLC) and liquid chromatography–mass spectrometry (LC–MS) protocols.

  • Format: Capsules
  • Strength: 500 mcg per capsule
  • Count: 60 capsules per bottle
  • Verified Purity: >99% (HPLC, LC–MS)
  • Container: Sealed amber bottle
  • Documentation: Batch-specific Certificate of Analysis (COA) available

Storage, handling, intended-use, and regulatory information are provided in the corresponding tabs on this product page.

References

  1. Hsieh MJ, Liu HT, Wang CN, et al. Therapeutic potential of pro-angiogenic BPC157 is associated with VEGFR2 activation and up-regulation. J Mol Med (Berl). 2017;95(3):323-333. doi:10.1007/s00109-016-1488-y
  2. Chang CH, Tsai WC, Lin MS, Hsu YH, Pang JHS. The promoting effect of pentadecapeptide BPC 157 on tendon healing involves tendon outgrowth, cell survival, and cell migration. J Appl Physiol (1985). 2011;110(3):774-780. doi:10.1152/japplphysiol.00945.2010
  3. Krivic A, Anic T, Seiwerth S, Huljev D, Sikiric P. Achilles detachment in rat and stable gastric pentadecapeptide BPC 157: promoted tendon-to-bone healing and opposed corticosteroid aggravation. J Orthop Res. 2006;24(5):982-989. doi:10.1002/jor.20096
  4. Cerovecki T, Bojanic I, Brcic L, Radic B, Vukoja I, Seiwerth S, Sikiric P. Pentadecapeptide BPC 157 (PL 14736) improves ligament healing in the rat. J Orthop Res. 2010;28(9):1155-1161. doi:10.1002/jor.21107
For research use only. Not for human consumption.