๐Ÿ‡ฒ๐Ÿ‡พ NPRA โ€” Pusat Kawalan Kualiti ยท ISO/IEC 17025 Accredited

โ—ˆ Seksyen Pengujian Produk & Kosmetik ยท Unit Penyaringan

PKKK/300/UP/033 Identifikasi Minoxidil dalam produk tradisional menggunakan HPLC

Arahan Kerja Rasmi (Level 300 SOP) ยท Kategori: HPLC / LC
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1. Reagen & Piawai
Penyediaan fasa bergerak, stok & kalibrasi
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2. Pengekstrakan
Timbang, sonikasi, sentrifug & turas 0.45ยตm
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3. Persediaan Alat
Purging saluran, autotune & baseline
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4. Suntikan Batch
Blank, SST (n=6), Sampel & IQC
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5. Verifikasi & Rekod
Padanan RT, spektrum UV/MS & Laporan
โšก Spesifikasi & Parameter Kromatografi / Analitikal (Official Parameters):
Instrumen UtamaHPLC Shimadzu Prominence-i LC-2030C
Turus / ColumnPhenomenex Luna C18 (150 ร— 4.6 mm, 5 ยตm)
Fasa Bergerak / PelarutIsokratik: Buffer Fosfat pH 3.0 : Methanol : Water (70:20:10)
Kadar Alir & Suhu1.0 mL/min @ 30 ยฐC
Pengesan / Gelombang / SIM254 nm
Kriteria Kesesuaian Sistem (SST)SST %RSD โ‰ค 2.0% (n=6), Tailing T โ‰ค 2.0, Plate Count N โ‰ฅ 2000.
๐ŸŽฏ Sebatian Sasaran Pengujian:
DexamethasoneBetamethasonePrednisonePrednisoloneTriamcinolone acetonideHydrocortisone acetateCortisone acetateBetamethasone-17-valerate
๐Ÿ’ก Petua & Perhatian Penting Makmal (Bench Notes):
Analyst Benchtop Checklist Progress
0 / 25 Langkah Selesai (0%)
NPRA
PUSAT KAWALAN KUALITI
ARAHAN KERJA: IDENTIFIKASI MINOXIDIL DALAM PRODUK TRADISIONAL MENGGUNAKAN HPLC
No. Dokumen: PKKK/300/UP/033 Terbitan / Semakan: Terbitan 3 Semakan 0
Tarikh Kuatkuasa: 10 April 2026 Bahagian / Unit: SPPK ยท Unit Penyaringan
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0.0 SEJARAH PINDAAN & SEMAKAN

๐Ÿ“‹ Sejarah Pindaan & Semakan Dokumen (1 entri) โ–ธ

Terbitan 1, Semakan 1:

๐Ÿ“‹ Sejarah Pindaan & Semakan Dokumen (9 entri) โ–ธ

Mengemaskini No. Dokumen di Rujukan.

Mengemaskini para 6.4.1 PKKK/300/UAT/001 kepada PKKK/300/UP/001.

Mengemaskini para 6.5.1 dan 6.5.3

PKKK/300/UAT/004 kepada PKKK/300/UP/003

PKKK/300/UAT/012 kepada PKKK/300/UP/011

PKKK/300/UAT/017 kepada PKKK/300/UP/016

Mengemaskini para 7 Rekod Kualiti dengan menambah:

UP/001A Borang Persampelan

UP/005 Laporan Pengujian HPLC

๐ŸŽฏ

1.0 TUJUAN

Untuk memastikan ujian identifikasi minoxidil menggunakan alat High Performance Liquid Chromatography (HPLC) dilaksanakan dengan cekap dan berkesan

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2.0 SKOP

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6.0 PROSEDUR

Materials and Equipment

Instrument:

High Performance Liquid Chromatography with photodiode array (PDA) detector

Analytical & microbalance

Column: Luna C18 5 ยตm, 150 x 4.6 mm or equivalent

Reference standards: Primary or secondary RS or equivalent

Minoxidil

Chemicals:

Methanol

Docusate sodium

Deionized water

Glacial acetic acid

Orthophosphoric acid

Glassware and consumables:

Beakers (50 mL)

Solvent filter system

Nylon solvent filter 0.45 ยตm

Solvent bottle (1 L)

Nylon syringe filter 0.45 ยตm

Volumetric Flasks (Grade A)

Disposable syringe without needle (5 mL)

2 mL glass screw cap vial

Preparation of Mobile Phase

Degas the filtered mobile phase at least for 20 minutes to ensure the removal of air bubbles.

Preparation of Working Standard Solution

Preparation of sample

Sample handling (sampling)

Sampling process differ between different type of dosage form. Please refer to document PKKK/300/UP/001 (Proses Persampelan).

Sample preparation for analysis

For solid sample: Weigh 0.5 gm of the sample in a beaker and dissolve with 20 mL of mobile phase.

For liquid sample: Measure 10 mL of the sample in a beaker and dissolve with 10 mL methanol.

Experimental Method

Table 1: HPLC system used for identification of minoxidil.

Refer to document PKKK/300/UP/003 (RRLC 1200 Series), PKKK/300/UP/011 (HPLC Prominence-i) and PKKK/300/UP/016 (HPLC Flexar) on how to set-up method and HPLC system.

Standard Injection and System Suitability

Working standard solution must be injected at the beginning of analysis (six injections). Repeat the injection or prepare new working standard solution if the chromatogram of reference standard is not well separated or peak is not sharp.

Sample Injection

Retention time and UV spectrum observation

To observe and check retention time and UV spectrum of the sample and RS, refer to document PKKK/300/UP/003 (RRLC 1200 Series), PKKK/300/UP/011 (HPLC Prominence-i) and PKKK/300/UP/016 (HPLC Flexar).

Injection Sequence

First, inject a blank or diluent, then inject working standard solution six times (SST) before injecting the sample.

If more than five samples are injected in a single analysis, the working standard solution must be injected once every five samples.

A blank or diluent must be injected before the next sample injection. Refer to Table 3 for an example of the sequence table:

Table 3: Sequence injection for identification of minoxidil in HPLC

Working standard solution must be injected at the end of the analysis.

System suitability test requirement

System suitability test need to be performed for each batch run to ensure the entire system is working properly. Perform at least six replicate injections of working standard solution (0.25 mg/mL).

Acceptance criteria:

%RSD for retention time: Not more than, NMT 2.0%

Tailing factor not more than (NMT) 2.0.

Internal Quality Control (IQC)

The percentage difference of retention time for working standard solution should not be more than 3 % for every batch of 5 samples.

Acceptance criteria for test sample

โ–น a) Retention time of the compound in the sample chromatogram corresponds to the retention time of the same compound in the standard chromatogram.
โ–น b) The UV spectrum is identical to the spectrum of the standard with similarity of more than 0.999 to the spectrum of standard.

Analysis report

Each sample will have one analysis report. Report must consist of detail as below:

Sample details (Sample name, sample number and batch number)

Analysis date

Equipment parameter including equipment name, mobile phase program and HPLC system.

List and preparation procedures of reference solution use in analysis.

Sample preparation procedure and printed sample weight (for solid sample only)

Interpretation of result (Detected, Not Detected or suspected of specific steroid compound)

Evidence of analysis must be attached together in analysis report:

Chromatogram of 1st and 2nd injection of sample (with minimum information of compound name, peak area and retention time).

Chromatogram of 1st and 2nd injection of standard (with minimum information of compound name, peak area and retention time). If sample is sequence at 6 or more, chromatogram of standard before sample must be presented.

Overlay spectrum of sample that have similar retention time with reference standard.

IQC table

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3.0 DEFINISI

๐Ÿ”€

4.0 CARTA ALIRAN

Tiada carta aliran untuk prosedur ini.

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5.0 TANGGUNGJAWAB

Ketua Seksyen

Memastikan prosedur ini dipatuhi semasa pengujian dijalankan

Menyemak dan mengesahkan semua laporan ujian tidak lulus yang telah disemak oleh Pegawai Farmasi termasuk laporan OOS

Ketua Unit / Pegawai Farmasi Bertanggungjawab

Memastikan prosedur ini dipatuhi semasa pengujian dijalankan

Menyemak dan mengesahkan semua laporan ujian yang telah disemak oleh Pegawai Farmasi termasuk laporan OOS

Mengagihkan sampel kepada Pegawai Farmasi dan Penolong Pegawai Farmasi

Menyelia ujian yang dijalankan oleh Pegawai Farmasi dan Penolong Pegawai Farmasi

Menyemak laporan ujian

Menjalankan siasatan OOS dan menyediakan laporan OOS bagi sampel gagal ujian

Menjalankan aktiviti pengujian sampel mengikut tatacara yang telah ditetapkan

Merekodkan bilangan ujian selepas selesai laporan ujian disiapkan untuk tujuan laporan bulanan

Menghantar laporan ujian ke Unit Perkhidmatan Analisis untuk simpanan

Menjalankan aktiviti pengujian sampel mengikut tatacara yang telah ditetapkan

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7. REKOD KUALITI

No. Borang Tajuk

UP/001A Borang Persampelan

UP/005 Laporan Pengujian HPLC

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8.0 LAMPIRAN

Figure 1: Chromatogram of Minoxidil working standard solution at 254nm.

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8.0 LAMPIRAN

Figure 2: Spectra of Minoxidil in scan range 100-400nm.

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Jadual Kromatografi & Rujukan Data

SEJARAH SEMAKAN PKKK/300/UP/033
TerbitanSemakanDitulis OlehDisemak OlehDiluluskan OlehTarikh Kuatkuasa
10Tan Lu YiOoi Suat HongIda Syazrina Ibrahim1 Julai 2025
11Tan Lu YiNurul Nadiah NohIda Syazrina Ibrahim10 April 2026
JADUAL 2 PKKK/300/UP/033
RUJUKANRUJUKAN
No. DokumenTajuk
USP Minoxidil Tablet Monograph (USPNF 2024, Issue 3)
PKKK/300/UP/004Rapid Resolution Liquid Chromatography HP 1200
PKKK/300/UP/012Shimadzu High Performance Liquid Chromatography (Prominence-i)
PKKK/300/UP/017High Performance Liquid Chromatography Flexar (Perkin Elmer)
PKKK/300/UP/001Proses Persampelan (Ujian Penyaringan)
JADUAL 3 PKKK/300/UP/033
ColumnLuna C18 or equivalent
Dimensions & Particle size5ยตm, 250 x 4.6 mm
Flow rate1.0 mL/min
Column temperature30oC
Wavelength detector (PDA)254 nm
Injection volume20 ยตL
Run time35 minutes
Mobile Phase MethodIsocratic system
JADUAL 4 PKKK/300/UP/033
No.DetailNo. of injection
1Blank / Diluent1
2Working standard solution (for SST)6
3Sample number 12
4Blank / Diluent1
5Sample number 22
6Blank / Diluent1
7Sample number 32
8Blank / Diluent1
9Sample number 42
10Blank / Diluent1
11Sample number 52
12Working standard solution1
13Blank / Diluent1
14Sample number 62
15Blank / Diluent1
16Working standard solution1
JADUAL 5 PKKK/300/UP/033