PKKK/300/UP/033 Identifikasi Minoxidil dalam produk tradisional menggunakan HPLC
- Tapis semua fasa bergerak (akueus dan organik) menggunakan penuras membran 0.45 ยตm dan degas dalam kukus ultrasonik selama sekurang-kurangnya 15โ20 minit.
- Lakukan Auto Purge / Manual Purge setiap kali pelarut ditambah atau ditukar jenis bagi menyingkirkan buih udara.
- Pastikan garisan dasar (baseline) dan tekanan pam stabil (RSD < 2%) sebelum memulakan suntikan sampel kelompok.
- Bagi sampel matriks kapsul lembut (softgel), gunakan Chloroform kerana gelatin/minyak tidak larut dalam Methanol.
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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 | |
0.0 SEJARAH PINDAAN & SEMAKAN
Sejarah Pindaan & Semakan Dokumen (1 entri) โธ
Terbitan 1, Semakan 1:
Sejarah Pindaan & Semakan Dokumen (9 entri) โธ
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
1.0 TUJUAN
Untuk memastikan ujian identifikasi minoxidil menggunakan alat High Performance Liquid Chromatography (HPLC) dilaksanakan dengan cekap dan berkesan
2.0 SKOP
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
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
3.0 DEFINISI
4.0 CARTA ALIRAN
Tiada carta aliran untuk prosedur ini.
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
7. REKOD KUALITI
No. Borang Tajuk
UP/001A Borang Persampelan
UP/005 Laporan Pengujian HPLC
8.0 LAMPIRAN
Figure 1: Chromatogram of Minoxidil working standard solution at 254nm.
8.0 LAMPIRAN
Figure 2: Spectra of Minoxidil in scan range 100-400nm.
Jadual Kromatografi & Rujukan Data
| Terbitan | Semakan | Ditulis Oleh | Disemak Oleh | Diluluskan Oleh | Tarikh Kuatkuasa |
|---|---|---|---|---|---|
| 1 | 0 | Tan Lu Yi | Ooi Suat Hong | Ida Syazrina Ibrahim | 1 Julai 2025 |
| 1 | 1 | Tan Lu Yi | Nurul Nadiah Noh | Ida Syazrina Ibrahim | 10 April 2026 |
| RUJUKAN | RUJUKAN |
|---|---|
| No. Dokumen | Tajuk |
| USP Minoxidil Tablet Monograph (USPNF 2024, Issue 3) | |
| PKKK/300/UP/004 | Rapid Resolution Liquid Chromatography HP 1200 |
| PKKK/300/UP/012 | Shimadzu High Performance Liquid Chromatography (Prominence-i) |
| PKKK/300/UP/017 | High Performance Liquid Chromatography Flexar (Perkin Elmer) |
| PKKK/300/UP/001 | Proses Persampelan (Ujian Penyaringan) |
| Column | Luna C18 or equivalent |
|---|---|
| Dimensions & Particle size | 5ยตm, 250 x 4.6 mm |
| Flow rate | 1.0 mL/min |
| Column temperature | 30oC |
| Wavelength detector (PDA) | 254 nm |
| Injection volume | 20 ยตL |
| Run time | 35 minutes |
| Mobile Phase Method | Isocratic system |
| No. | Detail | No. of injection |
|---|---|---|
| 1 | Blank / Diluent | 1 |
| 2 | Working standard solution (for SST) | 6 |
| 3 | Sample number 1 | 2 |
| 4 | Blank / Diluent | 1 |
| 5 | Sample number 2 | 2 |
| 6 | Blank / Diluent | 1 |
| 7 | Sample number 3 | 2 |
| 8 | Blank / Diluent | 1 |
| 9 | Sample number 4 | 2 |
| 10 | Blank / Diluent | 1 |
| 11 | Sample number 5 | 2 |
| 12 | Working standard solution | 1 |
| 13 | Blank / Diluent | 1 |
| 14 | Sample number 6 | 2 |
| 15 | Blank / Diluent | 1 |
| 16 | Working standard solution | 1 |